COROENT THORACOLUMBAR IMPLANTS

K140659 · Nu Vasive, Incorporated · MAX · Jun 26, 2014 · Orthopedic

Device Facts

• Record ID: K140659
• Device Name: COROENT THORACOLUMBAR IMPLANTS
• Applicant: Nu Vasive, Incorporated
• Product Code: MAX · Orthopedic
• Decision Date: Jun 26, 2014
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 888.3080
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

The NuVasive® CoRoent® Thoracolumbar Implants are devices indicated for the following: Intervertebral Body Fusion The NuVasive CoRoent Thoracolumbar Implants are indicated for intervertebral body fusion of the spine in skeletally mature patients. The implants are designed for use with autogenous bone graft to facilitate fusion and supplemental internal spinal fixation system cleared by the FDA for use in the thoracolumbar spine. The devices are to be used in patients who have had at least six months of non-operative treatment. Thoracic Spine: The CoRoent Thoracolumbar Implants are intended for use for thoracic interbody fusions at one or two contiguous levels in the thoracic spine, from T1-T2 to T11-T12, or at the thoracolumbar junction (T12-L1), following discectory for the treatment of a symptomatic disc degeneration (DDD), including thoracic disc herniation (myelopathy and/or radiculopathy with or without axial pain). Lumbar Spine: The CoRoent Thoracolumbar Implants are intended for use at either one level or two contiguous levels in the lumbar spine, from L1-L2 to L5-S1, for the treatment of degenerative disc disease (DDD) with up to Grade I spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. Partial Vertebral Body Replacement The NuVasive CoRoent Thoracolumbar Implants may also be used as a partial vertebral body replacement device indicated for use in the thoracolumbar spine (T1 to L5) to replace a diseased or damaged vertebral body caused by tumor or fracture, to restore height of a collapsed vertebral body, and to achieve decompression of the spinal cord and neural tissues. The implants are intended to be used with supplemental internal spinal fixation systems (e.g. pedicle screw system) that are cleared by the FDA for use in the thoracic and lumbar spine. Allograft or autograft material may be used at the surgeon's discretion.

Device Story

CoRoent Thoracolumbar Implants are spinal interbody fusion and partial vertebral body replacement devices. Implants are available in various shapes/sizes to accommodate patient anatomy. Used in thoracic and lumbar spine to facilitate fusion or restore vertebral height following tumor/fracture. Requires supplemental internal spinal fixation (e.g., pedicle screws). Surgeon implants device during spinal surgery to achieve decompression and stabilization. Benefits include spinal height restoration and fusion support for patients with DDD or vertebral damage.

Clinical Evidence

Clinical performance data presented to support expanded indications for use in the thoracic spine. Data demonstrates no new types of safety or effectiveness questions.

Technological Characteristics

Materials: PEEK-Optima LT-1 (ASTM F2026) or titanium alloy Ti-6Al-4V (ASTM F136). PEEK implants include titanium alloy radiographic markers (ASTM F136 or F1472). Mechanical intervertebral body fusion/fixation device.

Indications for Use

Indicated for skeletally mature patients requiring intervertebral body fusion or partial vertebral body replacement in the thoracic (T1-T12) or lumbar (L1-S1) spine. Conditions include symptomatic degenerative disc disease (DDD), thoracic disc herniation, Grade I spondylolisthesis, tumor, or fracture. Requires at least six months of failed non-operative treatment for DDD. Used with supplemental internal spinal fixation and bone graft (autograft/allograft).

Regulatory Classification

Identification

An intervertebral body fusion device is an implanted single or multiple component spinal device made from a variety of materials, including titanium and polymers. The device is inserted into the intervertebral body space of the cervical or lumbosacral spine, and is intended for intervertebral body fusion.

Special Controls

*Classification.* (1) Class II (special controls) for intervertebral body fusion devices that contain bone grafting material. The special control is the FDA guidance document entitled “Class II Special Controls Guidance Document: Intervertebral Body Fusion Device.” See § 888.1(e) for the availability of this guidance document.(2) Class III (premarket approval) for intervertebral body fusion devices that include any therapeutic biologic (e.g., bone morphogenic protein). Intervertebral body fusion devices that contain any therapeutic biologic require premarket approval. (c) *Date premarket approval application (PMA) or notice of product development protocol (PDP) is required.* Devices described in paragraph (b)(2) of this section shall have an approved PMA or a declared completed PDP in effect before being placed in commercial distribution.

Predicate Devices

• NuVasive CoRoent System (K071795)
• NuVasive CoRoent Titanium System (K120918)
• NuVasive CoRoent Sterile Implants System (K132601)

Submission Summary (Full Text)

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Image /page/0/Picture/1 description: The image shows the logo for "NUVASIVE". To the left of the company name is an abstract graphic. Below the company name is the text "Speed of Innovation" in a smaller font size.

510(k) Premarket Notification K140659 NuVasive® CoRoent® Thoracolumbar Implants

JUN 2 6 2014

## 510(k) Summarv

In accordance with Title 21 of the Code of Federal Regulations, Part 807, and in particular 21 CFR \$807.92, the following summary of information is provided:

#### Submitted by: A.

Olga Lewis Regulatory Affairs Specialist NuVasive, Incorporated 7475 Lusk Blvd. San Diego, California 92121 Telephone: [phone]

Date Prepared: June 25, 2014

#### B. Device Name

| Trade or Proprietary Name: | <i>NuVasive</i> ® <i>CoRoent</i> ® <i>Thoracolumbar Implants</i> |
|----------------------------|------------------------------------------------------------------------------------|
| Common or Usual Name: | Intervertebral Body Fusion Device; Spinal Intervertebral<br>Body Fixation Orthosis |
| Classification Name: | Intervertebral Body Fusion Device; Spinal Intervertebral<br>Body Fixation Orthosis |

| Device Class: | Class II |
|-----------------|----------------------------------|
| Classification: | 21 CFR § 888.3080 and § 888.3060 |
| Product Code: | MAX, PHM, MQP |

#### C. Predicate Devices

The subject NuVasive CoRoent Thoracolumbar Implants are substantially equivalent to the predicate devices. NuVasive CoRoent System (K071795). NuVasive CoRoent Titanium System (K120918) and NuVasive CoRoent Sterile Implants System (K132601).

#### D. Device Description

The CoRoent Thoracolumbar Implants are manufactured from PEEK-Optima® LT-1 conforming to ASTM F2026 or titanium alloy (Ti-6Al-4V) conforming to ASTM F136. The PEEK device contains titanium alloy radiographic markers conforming to ASTM F136 or ASTM F1472. The implants are available in a variety of different shapes and sizes to suit the individual pathology and anatomical conditions of the patient. The device is intended to be used with supplemental internal spinal fixation systems that are cleared by the FDA for use in the thoracolumbar spine. This 510(k) is to expand the indications for use to include interbody fusion in the thoracic spine.

#### E. Intended Use

The NuVasive® CoRoent Thoracolumbar Implants are devices indicated for the following:

## Intervertebral Body Fusion

The NuVasive CoRoent Thoracolumbar Implants are indicated for intervertebral body fusion of the spine in skeletally mature patients. The implants are designed for use with autogenous bone graft to facilitate fusion and supplemental internal spinal fixation system cleared by the FDA for

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Image /page/1/Picture/1 description: The image shows the logo for Nuvasive. The logo consists of a stylized, abstract shape on the left, followed by the word "NUVASIVE" in a simple, sans-serif font. Below the company name, there is a tagline that reads "1Speed of Innovation" in a smaller font size. The logo is simple and modern.

use in the thoracolumbar spine. The devices are to be used in patients who have had at least six months of non-operative treatment.

## Thoracic Spine:

The CoRoent Thoracolumbar Implants are intended for use for thoracic interbody fusions at one or two contiguous levels in the thoracic spine, from T1-T2 to T11-T12, or at the thoracolumbar junction (T12-L1), following discectory for the treatment of a symptomatic disc degeneration (DDD), including thoracic disc herniation (myelopathy and/or radiculopathy with or without axial pain).

#### Lumbar Spine:

The CoRoent Thoracolumbar Implants are intended for use at either one level or two contiguous levels in the lumbar spine, from L1-L2 to L5-S1, for the treatment of degenerative disc disease (DDD) with up to Grade I spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.

### Partial Vertebral Body Replacement

The NuVasive CoRoent Thoracolumbar Implants may also be used as a partial vertebral body replacement device indicated for use in the thoracolumbar spine (T1 to L5) to replace a diseased or damaged vertebral body caused by tumor or fracture, to restore height of a collapsed vertebral body, and to achieve decompression of the spinal cord and neural tissues. The implants are intended to be used with supplemental internal spinal fixation systems (e.g. pedicle screw system) that are cleared by the FDA for use in the thoracic and lumbar spine. Allograft or autograft material may be used at the surgeon's discretion.

#### Technological Characteristics F.

As was established in this submission, the subject NuVasive CoRoent Thoracolumbar Implants are substantially equivalent to other predicate devices cleared by the FDA for commercial distribution in the United States. There have been no design changes to the implants previously cleared in the predicate 510(k)s. The subject device was shown to be substantially equivalent and have equivalent technological characteristics to its predicate device through comparison in areas including design, labeling/intended use, material composition, and function.

#### G. Performance Data

To establish substantial equivalence with predicate devices for the expanded indications for use. clinical performance data is presented. These data demonstrate that there are no new types of safety or effectiveness questions for the device in the expanded indications for use in the thoracic spine.

The results demonstrate that the subject NuVasive Thoracolumbar Implants are substantially equivalent to the predicate devices.

#### H. Conclusions

Based on the technological characteristics, comparison to predicate devices, and clinical performance data, the subject NuVasive CoRoent Thoracolumbar Implants has been shown to be substantially equivalent to legally marketed predicate devices.

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## DEPARTMENT OF HEALTH & HUMAN SERVICES

#### Public Health Service

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

June 26, 2014

Nuvasive, Incorporated Ms. Olga Lewis Regulatory Affairs Specialist 7475 Lusk Boulevard San Diego, California 92121

Re: K140659

Trade/Device Name: Nuvasive® CoRoent® Thoracolumbar Implants : Regulation Number: 21 CFR 888.3080 Regulation Name: Intervertebral body fusion device Regulatory Class: Class II Product Code: MAX, PHM, MQP Dated: May 28, 2014 Received: May 29, 2014

Dear Ms. Lewis:

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 - Ms. Olga Lewis

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 contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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/ReportalProblem/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 Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely yours.

# Ronald P. Jéan -S for

Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration

## Indications for Use

510(k) Number (if known)

#### K140659

#### Device Name

NuVasive® CoRoent® Thoracolumbar Implants

#### Indications for Use (Describe)

The NuVasive® CoRoent® Thoracolumbar Implants are devices indicated for the following:

#### Intervertebral Body Fusion

The NuVasive CoRoent Thoracolumbar Implicated for intervertebral body fusion of the spine in sketally mature patients. The implants are designed for use with autogenous bone graft to facilitate fusion and supplemental internal spinal fixation system cleared by the FDA for use in the thoracolumbar spine. The devices are to be used in patients who have had at least six months of non-operative treatment.

## Thoracic Spine:

The CoRoent Thoracolumbar Implants are intended for use for thoracic interbody fusions at one or two contiguous levels in the thoracic spine from T1-T2 to T11-T12, or at the thoracolumbar junction (T12-L1), following discectory for the treatment of a symptomatic disc degeneration (DDD), including thoracic disc hemiation (myelopathy and/or radiculopathy with or without axial pain).

### Lumbar Spine:

The CoRoent Thoracolumbar Implants are intended for use at either one level or two contiguous levels in the lumbar spine, from L1-L2 to L5-S1, for the treatment of degenerative disc disease (DDD) with up to Grade I spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.

### Partial Vertebral Body Replacement

The NuVasive CoRoent Thoracolumbar Implants may also be used as a partial vertebral body replacement device indicated for use in the thoracolumbar spine (T) to LS) to replace a diseased or damaged vertebral body caused by tumor or fracture, to restore height of a collapsed vertebral body, and to achieve decompression of the spinal cord and neural tissues. The implants are intended to be used with supplemental internal spinal fixation systems (e.g. pedicle screw system) that are cleared by the FDA for use in the thoracic and lumbar spine. Allograft or autograft may be used at the surgeon's discretion.

Type of Use (Select one or both, as applicable)

2 Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use (21 CFR 801 Subpart C)

## PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.

### FOR FDA USE ONLY

Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)

ine in skeletally

Expiration Date: January 31, 2017 See PRA Statement below.

Form Approved: OMB No. 0910-0120

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