UPTC SpineMED S200B Quick start guide

ADVANCED MEDICAL TECHNOLOGY
ModelS200B/S200C
OPERATIONAL INSTRUCTION MANUAL
Serial No.: Table: #____________________
Serial No.: Console: #__________________
Serial No.: Cervical: #__________________
Copyright © 2009 Universal Pain Technology Canada Inc. All rights reserved.
SpineMED® Patent #7201729
UPTC-WI-065 (A-Series)
v1.7
Version 1.7 October 30, 2015

WI-065 v1.7 ii
Table of Contents
Introduction to Universal Pain Technology Canada and the SpineMED® ....................................................1
1. Therapeutic Guidelines and Protocol.................................................................................................3
1.1 Review of Underlying Principles of the SpineMED® Procedure...........................................3
1.2 Indications and Contraindications for Patients of SpineMED® Procedure ...........................3
1.3 Guidelines for Patient Selection for SpineMED® Procedure ................................................4
1.4 Patient Instruction Prior to Undergoing the SpineMED® Procedure.....................................6
1.5 Standard Protocol for the SpineMED® Procedure................................................................6
1.6 Procedure Algorithm and Flowchart for SpineMED® Procedure........................................11
1.7 Recommended Adjuncts to the SpineMED® Procedure.....................................................12
1.8 Patient DO and DON’T ........................................................................................................12
1.9 Post SpineMED® Procedure Protocol.................................................................................13
2. Description of the SpineMED® System S200B/S200C....................................................................14
2.1 Intended Use of the SpineMED®........................................................................................14
2.2 Structural Design –Components and Features of the SpineMED® S200B/S200C...........14
2.3 Details of Individual Components of the SpineMED® System............................................19
2.4 Operational Design..............................................................................................................23
2.5 Accessories .........................................................................................................................25
2.6 Installation and Space Requirements..................................................................................26
2.7 SpineMED® Power On Procedure......................................................................................28
2.8 SpineMED® Shutdown Procedure......................................................................................29
3. SpineMED® Software Operation.......................................................................................................30
3.1 Operator Logon Screen.......................................................................................................30
3.2 Main Menu...........................................................................................................................31
3.3 Administration Menu Screen ...............................................................................................33
3.4 Patients Menu Screen .........................................................................................................34
3.5 Physician Menu Screen.......................................................................................................37
3.6 Users Menu .........................................................................................................................42
3.7 Database Management.......................................................................................................44
3.8 Logout/Exit...........................................................................................................................46
1.3.1 Contraindications 5
3.4.1 Enter New Patient .........................................................................................................34
3.4.2 Modify Existing Patient’s Information ............................................................................35
3.4.3 Archive or Restore Existing Patient Record..................................................................35
3.5.1 Enter New Physician.....................................................................................................38
3.5.2 Edit Existing Physician’s Information ............................................................................38
3.5.3 Physician’s Info Report .................................................................................................39
3.5.4 Physician’s List Report ..................................................................................................41
3.6.1 Enter New User.............................................................................................................43
3.6.2 Edit Existing User’s Information ....................................................................................44
3.7.1 Backup Database..........................................................................................................44
3.7.2 Restore Database .........................................................................................................45
3.7.3 Export Database............................................................................................................46

WI-065 v1.7 iii
4. Lumbar & Cervical Procedure Screens............................................................................................46
4.1 Lumbar Procedure Screen ..................................................................................................46
4.2 Cervical Procedure Screen .................................................................................................52
4.3 Reports Menu Screen..........................................................................................................58
4.4 Selecting Patient Data.........................................................................................................58
4.5 Report Options ....................................................................................................................60
5. Procedure Session .............................................................................................................................65
5.1 Review of Individual Modalities of Each Session................................................................65
5.2 Data Entry for Lumbar Session ...........................................................................................65
5.3 Data Entry for Cervical Session ..........................................................................................67
5.4 Instructions and Sequencing for Patient Set-up for Lumbar Session .................................67
5.5 Instructions and Sequencing for Patient Set-up for Cervical Session.................................72
6. Therapeutic Operational Guidelines.................................................................................................75
6.1 Outcome Measure Data Entry.............................................................................................75
7. Precautions .........................................................................................................................................75
7.1 Precautions for SpineMED® Procedure..............................................................................75
7.2 Precautions for Use of SpineMED® System.......................................................................76
7.3 Degree of Protection Against Harmful Ingress of Liquids: IPX0 (ordinary equipment)......76
7.4 Environmental Conditions for the Operation, Storage and Transport of the SpineMED®..77
8. Maintenance........................................................................................................................................77
8.1 Disposal of SpineMED® System.........................................................................................77
8.2 Regular Maintenance ..........................................................................................................77
8.3 Cleaning of Equipment........................................................................................................77
8.4 Service and Warranty..........................................................................................................78
8.5 Troubleshooting...................................................................................................................79
8.6 Power Troubleshooting and Fuse Replacement.................................................................80
9. Technical Specifications....................................................................................................................84
9.1 Power Supply ......................................................................................................................84
9.2 Dimensions and Weight.......................................................................................................85
9.3 Model Number Designation.................................................................................................85
9.4 Type B Applied Parts...........................................................................................................85
9.5 Compliance Standards........................................................................................................85
10. Manufacturer.......................................................................................................................................89
10.1 Contact Information.............................................................................................................89
10.2 European Union Authorized Representative.......................................................................90
10.3 United States Authorized Representative ...........................................................................90
10.4 Product Serial Label Example.............................................................................................90
APPENDIX..........................................................................................................................................................91
Device Classification........................................................................................................................91
Definition of Symbols.......................................................................................................................91
Warranty Certificate.........................................................................................................................92
4.5.1 Session Report..............................................................................................................60
4.5.2 Daily Progress Report...................................................................................................61
4.5.3 Patient Full Report.........................................................................................................63
4.5.4 Procedure Report..........................................................................................................64
8.6.1 Power Troubleshooting .................................................................................................80
8.6.2 Fuse Inspection.............................................................................................................83
9.5.1 Electromagnetic Standards EN 60601-1-2 2007 ..........................................................86
9.5.2 Electromagnetic Environment Guidance.......................................................................87
9.5.3 Compliance Standards Met...........................................................................................89

WI-065 v1.7 1
Introduction to Universal Pain Technology Canada and the SpineMED®
For the past 20 years, health care clinics throughout the world have been able to deliver a
non-invasive procedure for pain as a result of herniated, bulging, degenerative discs, facet
syndrome and failed back surgery. This non-surgical decompression* of discs has been
shown to be effective in reducing pain and improving the functional activity levels of patients.
Fortunately, the collection of experiences during this lengthy clinical history, now provide a
solid foundation for the improvements in the design and application of disc decompression.
Universal Pain Technology Canada was formed by a group of professionals from North America,
whose years experience with non-surgical disc decompression systems is unprecedented. Since
the 1980s, this group has been engaged in delivering and reviewing the results of decompression
and patient satisfaction. Recognition of the continued benefit of this procedure for the patients,
has served as motivation to work diligently on the engineering and manufacture of an enhanced
disc decompression device and the development of an effective procedure protocol.
The SpineMED® System (S200B/S200C) that is now in your possession is the new generation
decompression system by Universal Pain Technology Canada. The advances made have
culminated in a simplified, comfortable and efficient method of stabilizing the patient during
decompression while providing an accurate method of spinal joint distraction. In partnership with
the clinicians, the Universal Pain Technology Canada team has established a protocol that gives
the most consistent and reproducible effectiveness possible with disc decompression available
today. Together the technology and the knowledge of application create the SpineMED® System.
In the history of the manufacturing of medical technology, it has been demonstrated that the
effectiveness of a device is only a part of the procedure. How the professional uses the
technology is crucial to its success. It is the belief of UPTC that the delivery of a standardized
system of training and support is an integral part of the SpineMED® System and ensures the best
possible outcomes.
Initial training, online education and support are provided in the set-up and continue throughout
the operational phase of the S200B/S200C. Monitoring of the sessions, acts as a means of
continuous quality control. During the learning stage, the use of a method of standardized data
collection allows for the SpineMED® coordinator to view at any time a patient’s procedure plan
and outcome. Any changes required are offered to the clinician by direct feedback or via e-mail.
Upon completion of the training and testing, certification for use of the S200B/S200C is issued to
the professional Operator.
Universal Pain Technology Canada and its established network of resources will continuously
strive to provide the clinicians and the patients with the resources required to attain maximum
effectiveness, patient comfort, safety and efficiency of use for the clinician. Ongoing clinical
studies and customer feedback will provide the knowledge for necessary changes in the future.
This manual will serve as a guide for the health professionals who will be using the
SpineMED® System (S200B/S200C) and the SpineMED® Protocol for the Lumbar and
Cervical Spine. It is important that every Clinician and Operator of the SpineMED®
System read all of the instructions and warnings contained in this Manual, prior to
operation of the device.
*Spinal Decompression that is, unloading due to non-surgical distraction and positioning.

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CAUTION: FEDERAL LAW (CANADA/USA) RESTRICTS THIS DEVICE TO USE BY OR ON
ORDER OF A PHYSICIAN, CHIROPRACTOR, PHYSICAL THERAPIST OR PRACTITIONER
LICENSED TO USE THIS DEVICE. THIS EQUIPMENT MUST BE OPERATED/UTILIZED UNDER
THE DIRECT SUPERVISION OF A LICENSED HEALTHCARE PRACTITIONER.

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1. Therapeutic Guidelines and Protocol
1.1 Review of Underlying Principles of the SpineMED® Procedure
To be competent as clinicians working with the SpineMED® System,
it is essential to know the functional anatomy of the spine and the
surrounding tissues. This portion of the manual will serve to
highlight the principles that are significant to the delivery of
SpineMED® Decompression. The more detailed review of the
material required for learning will take place during the training
sessions once your SpineMED® System is installed. It is
recommended by UPTC that clinicians be trained and certified prior to
treatment of patients with the SpineMED® System.
The knowledge of how a normal disc operates as a shock absorber, how it remains
healthy, and, how it behaves under immense pressure, will provide you with the
foundation of the SpineMED® protocol. This information describes how the benefits of
the design of this particular system and the protocol for disc decompression; ultimately
provide pain relief for the patient.
The evolution of disc decompression has taken place over a long period of time, and
after a great deal of investigation. The scientific reference articles and studies are
strongly recommended, and are found in the Clinic Resource CD. Optimal
effectiveness is quickly reproducible when there is a consistency and accuracy in the
application technique with each patient. There is a routine that must be followed and
not varied with each patient. Although certain patients will require modification in the
delivery of the distraction, the basic principles apply. During the training and learning
stage, careful review of the results of each patient with an experienced Universal Pain
Technology Canada professional is extremely valuable.
1.2 Indications and Contraindications for Patients of SpineMED® Procedure
A) The Indications
SpineMED® is an inherently safe procedure; however, it must be performed on a
spinal column that is anatomically structurally stable. The standardized medical and
physiotherapy assessments completed prior to the patient entering into the procedure
provide the screening necessary for confirming the condition of the spine. It is strongly
recommended that prior to the SpineMED® procedure, the patient have the results of
a current spinal X-Ray (i.e. no less than 3 months old). If there are recent MRI or CAT
Scan diagnostics available, then it is up to the Clinician whether an x-ray is essential.
B) Candidates
a. The patient presenting with clinical and/ or radiological evidence of a herniated,
bulging or degenerative disc is ideal.

WI-065 v1.7 4
b. The patient clinically presenting with buttock, leg and foot pain as a result of Lumbar
spinal dysfunction, or shoulder, arm and hand pain as a result of Cervical spinal
dysfunction.
c. The patient presenting with classic nerve root involvement of Sciatica Radiculopathy.
d. Patients with lateral stenosis and central stenosis may respond if severe secondary
changes are not present in the vertebra and if the stenosis is not due to a structurally
narrow spinal canal.
e. Patients presenting with a pain pattern and clinically findings suggestive of facet
syndrome.
f. Patients presenting with back pain or neck pain and have degenerative disc findings,
which have been to other therapy numerous times, and were compliant with exercise
programs, but have not experienced pain relief.
g. Patients who have failed back surgery.
1.3 Guidelines for Patient Selection for SpineMED® Procedure
A) The maximum patient weight safe working load is 325 lbs.
B) Patients with lateral stenosis and central stenosis may respond if severe secondary
changes are not present in the vertebra. The definition of stenosis also becomes an
issue. When the diagnosis of stenosis results from an actual structural narrowing of
the spinal canal, in this situation, positive results are less likely. However, if the
diagnosis is present as a result of disc bulge, positive results can be expected.
C) The SpineMED® can be used post spinal surgery and following failed spinal surgery.
The use of SpineMED® in conjunction with percutaneous discectomy is not
contraindicated. Clinical trials have demonstrated that the dual approach seems to
offer an advantage especially in those patients who have more than one level of disc
herniation in which only the major segment was percutaneously excised.
Patients with a history of previous laminectomy may undergo the SpineMED®
procedure when the extent of surgical excision has not compromised the vertebral
articulations and ligamental structures. The guideline is that previous surgery is not
contraindicated unless there is hardware; i.e. wire mesh, screws, rods, etc., that have
been implanted in the spine. The procedure can be undertaken after 6 to 12 months
following the removal of the hardware to allow complete healing. The health care
professional and the Doctor will assess the time frame.
D) A patient with recurrent back or neck pain with little to no clinical findings presents a
challenge and often becomes a chronic pain patient with secondary gain issues. If the
patient continues to be motivated to alleviate the pain and does not want to continue
on with the use of pain medication, SpineMED® is a choice that can be presented to
the patient. The success rate with these patients is surprisingly high.

WI-065 v1.7 5
E) Although not a contra-indication, it is important to know if a patient is on narcotics for
pain relief prior to undergoing the procedure. A patient who has a long history of using
narcotics will be unable to accurately report a response to the procedure, and
depending on the drug, the patient is at risk for experiencing rebound pain.
F) It is necessary for patients with a history of narcotic use, to first discontinue narcotic
medication prior to beginning the procedure. If the patient has been on narcotics for a
short time and requires strong medication because of the pain level, the SpineMED®
procedure can begin while still taking narcotics for pain. In this scenario the narcotic
use should be closely monitored and curtailed as quickly as possible.
1.3.1 Contraindications
The SpineMED® Procedure should not be administered if any of the following
apply to the patient:
A) Pathological lesions or congenital deformities of the vertebral column that disrupt the
integrity and stability of the vertebral and ligamental structures.
B) Fractures; i.e. compression fractures within one year.
C) Patients with lateral stenosis and central stenosis may respond if severe secondary
changes are not present in the vertebra.
D) Neoplasm, spinal tumors; both metastasis and primary.
E) Spina bifida or pars defect.
F) Spondylolisthesis Grade 2 and greater.
G) Osteoporosis with more than 45% bone loss.
H) Progressive pathological or inflammatory process of the spinal joints or muscles.
I) Inflammatory diseases involving the Spine; i.e. Active Rheumatoid Arthritis or
Ankylosing Spondylitis.
J) Connective tissue disease; i.e. Scleroderma.
K) Cauda Equina Syndrome, which is a result of pressure on the cauda equina,
presenting with bowel and bladder dysfunction.
L) Post-surgical patient with hardware implants, including, but not limited to; rods, screw,
metal mesh implants in the spine.
M) Post-surgical patients who have had spinal surgery and healing of tissue is still required.
(The period of time post spinal surgery will vary between 6 months to a year).
N) Pregnancy
O) Patients under 15 years of age.

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1.4 Patient Instruction Prior to Undergoing the SpineMED® Procedure
Patients are instructed to read the Patient Handbook and to speak to the Clinician
about any questions or concerns. It is highly recommended that a patient complete a
clinic visit and observe the session in progress, if possible.
The patient must have available for their use an acceptable Lumbar support that they
must bring with them to the first session. The support serves primarily to prevent the
patient from participating in movements or activity, which will have a negative effect on
the healing that is taking place, and to offer some support to the Lumbar Spine. All
patients undergoing the SpineMED® procedure are advised to wear a Pelvic Support
Belt following each SpineMED® session. This is especially important if the patient
must travel any distance or may be subject to acceleration or deceleration forces in
transit. Pelvic Belts should also be worn when any postural strain is felt or anticipated
as well as whenever the patient engages in activities that may invoke Lumbar flexion
or rotational movements during the period of time they are on a course of SpineMED®
sessions. Also, many patients find that wearing a Pelvic Support Belt, especially after
a SpineMED® session, adds to their comfort level and assists them in maintaining a
regular regime of sessions, further facilitating their recovery.
The patient is told that the commitment to the procedure is vitally important and that
participation in strenuous activities and exercise during this time of healing will have a
definite negative effect upon the results of the procedure. There cannot be enough
encouragement given to the patient to comply too the suggested protocol and the “DO”
and “DON’T” instructions contained in the Patient Handbook. It is their part of the
program, which will have a direct effect on the outcome of the program. Patients are
asked to consider this as a time of healing like one would following an injury to any
joint.
Sessions are administered with patients fully clothed. However, comfortable, two-
piece clothing that can be separated at the waist and loosened at the wrist would be
the most practical and comfortable. To avoid bending immediately after each session,
it is advisable to wear shoes that slip-on, rather than lace up.
1.5 Standard Protocol for the SpineMED® Procedure
A) Completion of medical screening and review of previous medical records and
radiological reports. Minimal requirement is an X-Ray taken no longer than 3 months
ago. The Medical Screening Form and radiological records must be faxed or sent to
the SpineMED® Clinic, prior to the patient commencing the procedure.
B) The patient must review the Patient Handbook prior to beginning the procedure and is
encouraged to have any concerns dealt with prior to the sessions starting.
C) The patient will require a minimum of 20 sessions, which are administered daily, for a
minimum of 5 days each week. With each session, there is a cumulative effect. Each
SpineMED® session takes approximately 30 minutes, with total time for the session
taking 60 to 90 minutes, inclusive of adjunct modalities.

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D) The clinician reviews the Medical Screening Form, medical records and radiological
report at the first session. A standardized Physical Therapy Assessment is then
completed. It is important to review all the clinical information and confirm the patient
is an appropriate candidate.
E) Maximum Tension is calculated based on the patient’s body weight. Starting Tensions
should be 15% of Body weight. (*i.e. 160 lb. X 15% = 24 lb.) Gradual increase of
distraction forces are based on patient response to the session plus the general
guideline of 3-5 lbs. /session. Maximum distraction tensions of 15% of body weight +
25 lbs. is applicable to all patients. Most patients will find a comfortable plateau of
tensions at approximately 15% of body weight + 15 to 20 pounds. It is very rare that
tensions of 15% of body weight + 15 pounds is exceeded for any patient. The
SpineMED® will enter the calculated Maximum Tension for the first session; however,
the Operator can modify this value. Software will prevent User from entering
Maximum Tensions above 15% of body weight + 25 lbs
F) The SpineMED® software will alert the Operator in the event that they attempt to
increase the Maximum Tension beyond 15% of body weight + 15 pounds. The
following message will appear, to confirm that the Operator does wish to exceed the
typical protocol:
The SpineMED® software will also prevent the Operator from exceeding the maximum
recommended tensions for the patient being treated. If the Operator attempts to
exceed 15% of body weight + 25 pounds for a patient, the following error message will
appear:

WI-065 v1.7 8
G) Calculation of distractive force to be used for patients undergoing Cervical procedure.
Maximum Tension for Cervical procedure is calculated based on the patient’s gender.
Starting Tensions should be 4-5 lbs. for females and 5-6 lbs. for males. Tensions
should be increased by 1-2 lbs. daily, until optimum tensions are reached. The
SpineMED® software will prevent User from entering Maximum Tensions above 20lbs.
for females and 25 lbs. for males. Most male patients will reach a tension plateau of
15 lbs., while females will typically reach 12 lbs. The SpineMED® software will
calculate the Maximum Tension for the first session; however, the Operator can modify
this value.
The SpineMED® software will alert the Operator in the event that they attempt to
increase the Maximum Tension beyond 15 lbs. for females and 18 lbs. for males. The
following message will appear, to confirm that the Operator does wish to exceed the
typical protocol:
The SpineMED® software will also prevent the Operator from exceeding the maximum
recommended tensions for the patient being treated. If the Operator attempts to
exceed 20 lbs. for a female patient or 25 lbs for a male patient, the following error
message will appear:

WI-065 v1.7 9
H) Settings for variable Pelvic angles to target specific spinal segments are
programmable. The guidelines for targeting specific Lumbar segments are as
follows:
DISTRACTION ANGLES:
L5-S1 ................................................ 0 degrees
L5-S1, L4-L5 ..................................... 5 degrees
L4-5................................................. 10 degrees
L4-L5, L3-L4.................................... 15 degrees
L3-4................................................. 20 degrees
L3-L4, L2-L3.................................... 25 degrees
L2-3 and above............................... 25 degrees
I) Settings for variable Cervical angles to target specific spinal segments are
programmable. The guidelines for targeting specific Cervical segments are as
follows:
DISTRACTION ANGLES:
C1-C2 .......................................... 0 degrees
C1-C2, C2-C3.............................. 3 degrees
C2-C3 .......................................... 7 degrees
C2-C3, C3-C4.............................10 degrees
C3-C4 .........................................14 degrees
C3-C4, C4-C5.............................17 degrees
C4-C5 .........................................21 degrees
C4-C5, C5-C6.............................24 degrees
C5-C6 .........................................28 degrees
C5-C6, C6-C7.............................30 degrees
C6-C7 .........................................30 degrees
C7-T1..........................................30 degrees

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Each standard Lumbar session consists of the following
** Patient to sign release form before procedure started
DURATION
Completion of self-reported V.A.S. for pain Scale
5 min.
Infrared heat application to tissue surrounding the area to be
treated.
15 min. to 30 min.
Lumbar decompression with SpineMED® S200B/S200C
For details see Section 5
30 min.
Cryotherapy or conventional Ice Pack
10 min.
Pain Control Device—Interferential Current Unit
15 min.
Application of Lumbar Support
Continuous
Post Procedure completion of self reported V.A.S and Oswestry
Variable
Reinforcement of DO and DON’T after the Procedure

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1.6 Procedure Algorithm and Flowchart for SpineMED® Procedure

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1.7 Recommended Adjuncts to the SpineMED® Procedure
Non-Steroidal Anti-Inflammatory Drugs (NSAID):
To relieve associated localized soft tissue inflammation and irritation during a
SpineMED® session, it is important to select an NSAID agent that also possesses a
significant analgesic component. Clinical studies have shown evidence that intradiscal
pressures are reduced to negative levels during disc decompression, creating diffusion
gradients in excess of 200 mm/Hg. across Vertebral End Plates. Therefore, it has
been proposed that this diffusion gradient facilitates migration of serum levels of anti-
inflammatory compounds into intervertebral spaces and to the site of the intervertebral
lesions.
It is recommended that each candidate for the SpineMED® procedure be prescribed a
concomitant NSAID. A therapeutic dosage regime should be started 48 hours prior to
the first SpineMED® session in order to develop effective serum levels of anti-
inflammatory activity to reduce discomfort from the initial mobilization of irritated
Lumbar structures. The agent should be continued throughout the sessions and for
approximately two weeks thereafter. To reduce gastric irritations, all NSAID’s should
be taken with food.
Calcium Supplements:
Calcium is an essential element in the process of skeletal muscle relaxation. This
function is especially important for the "strut” (paravertebral) muscles that have a
tendency to react with spasms to Lumbar stimuli. Clinical studies have indicated that
patients seem to benefit with reduced incidence of spasms when they have a daily
intake greater than 800 mg. of elemental Calcium. The preferred source of elemental
Calcium is that from the organic salts such as Calcium Lactate or Calcium Gluconate
(if allergic to Lactate).
1.8 Patient DO and DON’T
Optimal results are achieved when patients follow the DO and DON'T of the
SpineMED® Program.
DO
DON’T
DO rest for at least 1 or 2 hours after each
session
DON’T bend forward for the first few
hours after a session
DO be aware of your sitting, standing, and
lying posture
DON’T twist your back
DO wear your SpineMED® low back support
as instructed
DON’T lift heavy objects (over 20 lbs.)
DO wear shoes without laces and use a long
handled shoe horn if necessary
DON’T wear high-heel shoes
DO report to the Therapist any change in your
symptoms at your next visit
DON’T walk long distances after a
session
DON’T try to engage in those activities
that you avoided before the procedure,
too soon after even though you feel relief

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1.9 Post SpineMED® Procedure Protocol
A) Exercise program: At an appropriate time, approximately 4 weeks following
completion of the procedure, an exercise program, specific to the patient’s condition
will be introduced. It will include stretches to promote flexibility through proper
alignment of the healing tissue, stabilization and strengthening exercises and range of
motion exercises. Throughout the course of the procedure, the client will be instructed
in proper body mechanics, posture, and the correct way of using the affected structure
to avoid re-injury.
B) Experience has shown that patients undergoing procedure for Posterior Facet
Syndromes may resume full activities immediately following remission of their
symptoms. However, those who have achieved remission from more serious Lumbar
or Cervical dysfunction that involve Intervertebral Discs such as herniations and/or
Degenerative Disc Disease, need to realize that their Lumbar/Cervical structures and
tissues need time to heal. Follow up of post program patients indicate that this
resolution period requires at least one to two months, before individuals can safely
engage in body contact sports or strenuous work and recreational activities. This
depends on the severity of the underlying lesions and needs to be discussed with the
Clinician.
C) In the immediate post procedure period when a patient is in remission and relieved of
pain, there is a tendency to return to a level of activity at work or play that is too
strenuous. If this is done, the patient is at risk of experiencing a relapse. Therefore, it
is especially important to allow time for resolution and healing of decompressed
Lumbar/Cervical Discs and the surrounding structures and tissues.
D) Following a course of SpineMED® sessions, patients in remission should be cautioned
to slowly increase their exercise program. If their low back pain has caused them to
restrict their activities in the past, their muscle strength might be decreased. In some
cases, muscles are smaller (atrophied) and weak as a result of nerve compression.
For at least one-month post session, exercises that cause flexion, extension or rotation
of the Lumbar/Cervical Spine need to be started in a gradual and cautious manner.
E) After patient has completed a minimum of twenty sessions, there should be regular
follow-up by one of the SpineMED® Health Care professionals at four weeks for re-
assessment and instruction of an exercise program. A review of patient’s exercises
should be completed within 2 months or earlier, if required. Individual issues can be
addressed. The Health Care professional should perform a 6 month and one year
follow-up at the SpineMED® clinic.
F) The majority of patients that recover through the SpineMED® procedure generally
remain in remission. Some individuals whose lifestyle or work environment exposes
them to higher risk factors have found that a maintenance program consisting of
occasional sessions is necessary. The Clinician will determine this, and the schedule
of these sessions will be decided upon at that time. Generally these sessions are
performed at one or two week intervals. The purpose of the maintenance sessions is
to serve as a measure of protection against disabling exacerbation of low back pain
syndrome. Patients in this category develop their own rhythm of maintenance visits
that keeps them free from problems.

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2. Description of the SpineMED® System S200B/S200C
2.1 Intended Use of the SpineMED®
The SpineMED® System provides a program of sessions for relief from pain for those
patients suffering with low back pain, neck pain or Sciatica. Each session consists of a
physician prescribed protocol period on the SpineMED® and is designed to provide static,
intermittent, and cycling distraction forces to relieve pressures on structures that may be
causing low back pain, neck pain or Sciatica. It relieves pain associated with herniated
discs, bulging or protruding discs, Degenerative Disc Disease, Posterior Facet Syndrome,
and Sciatica. It achieves these effects through decompression of intervertebral discs, that
is, unloading due to distraction and positioning.
2.2 Structural Design –Components and Features of the SpineMED® S200B/S200C
The SpineMED® System consists of 3 major components:
A) Computerized Console Unit with integrated Touchcomputer (S200B)
B) Distraction Table with Lumbar Decompression (S200B)
The Console Unit provides the power and the control systems to drive the function of the
SpineMED® System, where the Table is the functional component used for the
procedure. Together, the components function as one unit.
C) Cervical Component (S200C)
The Cervical Unit is a bolt-on component to the SpineMED® Table, and is controlled by
the Console Unit.

WI-065 v1.7 15
A) The Console Unit consists of:
1. Touchcomputer with proprietary software
2. UPS (Uninterruptible Power Supply) System
3. Laser Printer for report generation
2.
3.
1.
2.

WI-065 v1.7 16
A) The Console Unit consists of: (continued, side view)
4. System Power Switch
5. Main Supply Power Switch
6. Main Supply Power Cord
7. Fuse Holder
6.
5.
4.
7.
5.
Close up Image

WI-065 v1.7 17
B) The Table consists of:
1. A powered, moveable lower Table section
2. A tilting section incorporated into the lower moveable section, which allows tilting
of the Pelvis during distraction
3. Pelvic Restraints
4. Patient Hand Held Electrical Emergency Switch (aka Emergency/Panic Switch)
5. Crank Handle to adjust the Pelvic Restraints against the patient
6. Patient Monitor with incorporated CD/DVD Player for patient entertainment
7. Grab Handle for moving Table
8. Handle for lowering Table Feet
9. Inflating Bulb for Lumbar Air Bladder
10. Upper Restraint System Slack Removal Lever
11. Adjustable Knee Bolster Support Cushion
12. Headphone Hook
13. Cervical Unit (detailed in later section)
1.
2.
5.
6.
8.
3.
8.
7.
4.
9.
10.
9.
11.
13.
12.