EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM

K991092 · Electro-Biology, Inc. · KWQ · Apr 29, 1999 · Orthopedic

Device Facts

• Record ID: K991092
• Device Name: EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM
• Applicant: Electro-Biology, Inc.
• Product Code: KWQ · Orthopedic
• Decision Date: Apr 29, 1999
• Decision: SESE
• Submission Type: Special
• Regulation: 21 CFR 888.3060
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

The EBI SpineLink™ Anterior Cervical Spinal System is intended for anterior interbody screw fixation of the cervical spine at levels C3-C7. The System is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusions in patients with degenerative disc disease (as defined by neck pain of discogenic origin of the disc confirmed by patient history and radiographic studies), trauma (including fractures), tumors, deformity (defined as kyphosis, lordosis, or scoliosis), pseudarthrosis, and/or failed previous fusions. Warning: This device is not approved for screw attachment to the posterior elements (pedicles) of the cervical, thoracic, or lumbar spine.

Device Story

EBI SpineLink™ is a cervical spinal fixation system utilizing interconnecting links for anterior interbody screw fixation. This submission introduces a 4.5mm diameter bone anchor screw. The device is used by surgeons in clinical settings to provide temporary stabilization of the anterior spine during cervical fusion procedures. By securing the spinal segments, the system facilitates the development of spinal fusions, potentially alleviating symptoms associated with degenerative disc disease, trauma, tumors, or spinal deformities. The device is intended for prescription use only.

Clinical Evidence

Bench testing only. No clinical data provided.

Technological Characteristics

Cervical spinal fixation system consisting of interconnecting links and bone anchor screws. Features a 4.5mm diameter bone anchor screw. Mechanical fixation device; no energy source or software components. Materials and design are consistent with previously marketed spinal systems.

Indications for Use

Indicated for patients requiring temporary anterior cervical spine stabilization (C3-C7) during fusion development. Conditions include degenerative disc disease, trauma (fractures), tumors, deformity (kyphosis, lordosis, scoliosis), pseudarthrosis, and failed previous fusions. Contraindicated for posterior element (pedicle) attachment in cervical, thoracic, or lumbar spine.

Regulatory Classification

Identification

A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct “sway back,” scoliosis (lateral curvature of the spine), or other conditions.

Predicate Devices

• EBI SpineLink™ Anterior Cervical Spinal System
• Synthes® Cervical Spine Locking Plate

Submission Summary (Full Text)

{0}------------------------------------------------

4/29/99

K991092

## 510(k) Summary of Safety & Effectiveness

This 510(k) Summary of Safety and Effectiveness for the EBI SpineLink™ Anterior Cervical Spinal System is provided as required per Section 513(D)(3) of the Food, Drug and Cosmetic Act.

| 1. | Submitter: Electro-Biology, Inc.<br>100 Interpace Parkway<br>Parsippany, NJ 07054 | Contact Person: Jon Caparotta<br>Telephone: [phone] |
|----|-----------------------------------------------------------------------------------|------------------------------------------------------------|
|----|-----------------------------------------------------------------------------------|------------------------------------------------------------|

Date prepared: March 30, 1999

| 2. Proprietary Name: | EBI SpineLink™ Anterior Cervical Spinal System |
|-----------------------|------------------------------------------------|
| Common Name: | Spinal Fixation Device |
| Classification Names: | Spinal Intervertebral Body Fixation Orthosis |

- 3. Predicate or legally marketed devices that are substantially equivalent:
- · EBI SpineLink™ Anterior Cervical Spinal System
- · Synthes® Cervical Spine Locking Plate
- Description of the device: The EBI SpineLink™ System is a cervical spinal fixation 4. device that uses interconnecting links. This submission is for the addition of a 4.5mm diameter bone anchor screw.
- 5. Intended Use: The EBI SpineLink™ Anterior Cervical Spinal System is intended for anterior interbody screw fixation of the cervical spine at levels C3-C7. The System is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusions in patients with degenerative disc disease (as defined by neck pain of discogenic origin of the disc confirmed by patient history and radiographic studies), trauma (including fractures), tumors, deformity (defined as kyphosis, lordosis, or scoliosis), pseudarthrosis, and/or failed previous fusions.

Warning: This device is not approved for screw attachment to the posterior elements (pedicles) of the cervical, thoracic, or lumbar spine.

{1}------------------------------------------------

- 7. Comparison of the technological characteristics of the device to predicate devices: There are no significant differences between the EBI SpineLink™ Anterior Cervical Spinal System and other currently marketed spinal systems. It is substantially equivalent* to the predicate devices in regards to intended use, materials and function. Testing companing the modifications to the previous system demonstrated that the device complies with applicable standards and meets all of its functional requirements.
* Any satement made in conjunction with this submission of substantial equivalence to any other product is intended only to relate to whether the product can be lawfully market approval or reclassification and is not intended to be interpreted as an admission or any other type of evidence in patent infringement litigation. [Establishment Registration and Premarket Notification Procedures, Final Regulation, Preamble, August 23, 1977, FR 42520 (Docket No. 76N-0355.)]

{2}------------------------------------------------

Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, with flowing lines representing hair or clothing.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

APR 2 9 1990

Mr. Jon Caparotta Manager, Regulatory Affairs Electro-Biology, Inc. 100 Interpace Parkway 07054 Parsippany, New Jersey

Re: K991092 EBI SpineLink™ Anterior Trade Name: Cervical Spinal System Regulatory Class: II Product Code: KWQ March 29, 1999 Dated: Received: April 1, 1999

Dear Mr. Caparotta:

We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act of the Act. include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.

{3}------------------------------------------------

## Page 2 - Mr. Jon Caparotta

This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA findinq of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to
premarket notification" (21 CFR 807.97). Other gener Other qeneral information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number [phone] or [phone] or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".

Sincerely yours,

Witten, Ph.D., M.D. Cel a M. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{4}------------------------------------------------

## Statement of Indications for Use:

The EBI SpineLink™ Anterior Cervical Spinal System is intended for anterior interbody screw fixation of the cervical spine at levels C3-C7. The System is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusions in patients with degenerative disc disease (as defined by neck pain of discogenic origin of the disc confirmed by patient history and radiographic studies), trauma (including fractures), tumors, deformity (defined as kyphosis, or scoliosis), pseudarthrosis, and/or failed previous fusions.

WARNING: This device is not approved for screw attachment to the posterior elements (pedicles) of the cervical, thoracic, or lumbar spine.

Dolly

(Divisior General Restorative Devices 11991092 510(k) Number

Prescription Use
(Per 21 CFR 801.109) X