TRANSCORP TRANS-PLATE ANTERIOR CERVICAL PLATE SYSTEM

K092695 · Transcorp, Inc. · KWQ · May 21, 2010 · Orthopedic

Device Facts

• Record ID: K092695
• Device Name: TRANSCORP TRANS-PLATE ANTERIOR CERVICAL PLATE SYSTEM
• Applicant: Transcorp, Inc.
• Product Code: KWQ · Orthopedic
• Decision Date: May 21, 2010
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 888.3060
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

The Transcorp Trans-Plate Anterior Cervical Plate System is intended for anterior screw fixation of the cervical spine (C2-C7). These implants have been designed to provide stabilization to cervical fusion. Indications for the use of this implant system include degenerative disc disease (defined as neck pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), tumor, pseudarthrosis, or failed previous fusion. WARNING: The Transcorp Trans-Plate Anterior Cervical Plate System in not intended for screw attachment or fixation to the posterior elements (pedicles) of the cervical, thoracic or lumbar spine.

Device Story

Anterior cervical plate system for spinal stabilization; includes titanium alloy plates, bone screws, and PEEK cover plate. Device fixates vertebral bodies C2-C7 to facilitate fusion. Used by surgeons in clinical settings. Mechanical performance validated via static/dynamic bending and torsion testing per ASTM standards. Provides structural support to the cervical spine to aid healing in patients with degenerative or traumatic spinal conditions.

Clinical Evidence

No clinical data. Bench testing only, including static torsion, static bending compression, dynamic bending compression (ASTM F1717), and wear debris analysis (ASTM F1877).

Technological Characteristics

System components: Titanium alloy (ASTM F136-08) plates, screws, and locking blade; PEEK (ASTM F2026) cover plate. Mechanical fixation via screw-to-plate attachment to vertebral bodies. Non-active, implantable orthopedic device.

Indications for Use

Indicated for anterior screw fixation of cervical spine (C2-C7) to provide stabilization for fusion in patients with degenerative disc disease, spondylolisthesis, trauma (fracture/dislocation), spinal stenosis, deformities (scoliosis, kyphosis, lordosis), tumor, pseudarthrosis, or failed previous fusion. Contraindicated for posterior element (pedicle) fixation.

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

• Synthes CSLP (K030866)
• Medtronic Atlantis Cervical Plate System (K021461)

Submission Summary (Full Text)

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# 510(k) Summary Pursuant to 21 CFR 807.92c

Submitted By:

Andrew Rodenhouse Transcorp. Inc. 1000 100th St. SW Suite F Byron Center, MI 49315 Ph: 616-877-4177 Fax: [phone]

MAY 21 2010

Date:

May 20, 2010

Device Information:

Trade Name: Common Name: Classification:

Transcorp Trans-Plate Anterior Cervical Plate System Spinal Intervertebral Body Fixation Orthosis 21 CFR Section 888.3060, Product Code KWQ, Class II

Predicate Devices:

K030866 Synthes CSLP K021461 Medtronic Atlantis Cervical Plate System

#### Device Description:

The Transcorp Trans-Plate Anterior Cervical Plate System includes The Transoorp Trans Fivical plates and bone screws. The anterior cervical plate system includes a cover plate that covers the bone screws and the "window" of the plate. The cover plate is manufactured from implant grade PEEK conforming to ASTM F2026na. The plates, screws, and cover plate locking blade are manufactured from Titanium Alloy conforming to ASTM F136-08. The plate is fixated by attaching screws through holes in the plate to The plate is fixution of the vertebral body of the cervical spine (C2-C7).

510(k) Premarket Notifica

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#### Intended Use:

The Transcorp Trans-Plate Anterior Cervical Plate System is intended for anterior screw fixation of the cervical spine (C2-C7). These implants have been designed to provide stabilization to cervical fusion. Indications for the use of this implant system include degenerative disc disease (defined as neck pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), tumor, pseudarthrosis, or failed previous fusion.

WARNING: The Transcorp Trans-Plate Anterior Cervical Plate System in not intended for screw attachment or fixation to the posterior elements (pedicles) of the cervical, thoracic or lumbar spine.

#### Performance Data:

Performance testing was performed on the Transcorp Trans-Plate Anterior Cervical Plate System. Static torsion, static bending compression, and dynamic bending compression were performed per ASTM F1717. A wear testing analysis was performed to determine particulate generation and wear debris was collected and analyzed per ASTM F1877. No clinical testing was performed.

## Substantial Equivalence:

The Transcorp Trans-Plate Anterior Cervical Plate System is equivalent to the predicate devices in design, function, and indications for use. The results of non-clinical testing and analysis demonstrate that the mechanical performance of the Transcorp Trans-Plate Anterior Cervical Plate System is equivalent to the predicate devices. Thus, the Transcorp Trans-Plate Anterior Cervical Plate System is substantially equivalent to the predicate devices.

510(k) Premarket Notificatio

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Image /page/2/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" around the perimeter. In the center of the circle is an emblem that features a stylized eagle with three lines extending from its wing. The eagle is facing to the right.

Food and Drug Administration 10903 New Hampshire Avenue Document Mail Center - WO66-G609 Silver Spring, MD 20993-0002

### MAY 2 1 2010

Transcorp, Inc. % Mr. Andrew Rodenhouse Principle Engineer 1000 100th Street SW, Suite F Byron Center, Michigan 49315

Re: K092695

Trade/Device Name: Transcorp Trans-Plate Anterior Cervical Plate System Regulation Number: 21 CFR 888.3060 Regulation Name: Spinal intervertebral body fixation orthosis Regulatory Class: II Product Code: KWQ Dated: May 18, 2010 Received: May 19, 2010

Dear Mr. Rodenhouse:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate 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) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set

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Page 2 - Mr. Andrew Rodenhouse

forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

vards Fees/Resources for Industry Training

Sincerely yours.

Kaubaie Buelund

Mark N. Melke Director Division of Surgical, Orthopedic and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# Indications for Use Statement

K092695

510(k) Number:

Device Name:

Transcorp Trans-Plate Anterior Cervical Plate System

Indications for Use:

The Transcorp Trans-Plate Anterior Cervical Plate System is intended for anterior screw fixation of the cervical spine (C2-C7). These implants have been designed to provide stabilization to cervical fusion. Indications for the use of this implant system include degenerative disc disease (defined as neck pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), tumor, pseudarthrosis, or failed previous fusion.

WARNING: The Transcorp Trans-Plate Anterior Cervical Plate System in not intended for screw attachment or fixation to the posterior elements (pedicles) of the cervical, thoracic or lumbar spine.

| Prescription Use <u>X</u><br>(per CFR 801.109) | or |
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Over-the-counter use

Concurrence of CDRH, Office of Device Evaluation (ODE)

(Division Sign-Off) Division of Surgical, Orthopedic, and Restorative Devices

510(k) Number_________________________________________________________________________________________________________________________________________________________________