CoRoent
- Primary DI
- 00887517567352
- Brand
- CoRoent
- Company
- Nuvasive, Inc.
- Model
- 5180280
- Device description
- CoRoent Ant TLIF PEEK, 8x10x28mm 0°
- Published
- 2015-10-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MAX | Intervertebral fusion device with bone graft, lumbar |
| MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE |
| ODP | Intervertebral fusion device with bone graft, cervical |
| OVE | Intervertebral fusion device with integrated fixation, cervical |
| PHM | Intervertebral fusion device with bone graft, thoracic |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
| MQP | Spinal Vertebral Body Replacement Device | Orthopedic | 2 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | Orthopedic | 2 |
| OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical | Orthopedic | 2 |
| PHM | Intervertebral Fusion Device With Bone Graft, Thoracic | Orthopedic | 2 |
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K071795 | 000 | NUVASIVE COROENT SYSTEM | Nuvasive, Inc. | 2007-12-04 | MAX |
| K081611 | 000 | NUVASIVE COROENT SYSTEM | Nuvasive, Inc. | 2008-10-02 | ODP |
| K140659 | 000 | COROENT THORACOLUMBAR IMPLANTS | Nu Vasive, Incorporated | 2014-06-26 | MAX |
| K141665 | 000 | NuVasive CoRoent System | Nuvasive, Inc. | 2015-03-13 | MAX |
| K150994 | 000 | NuVasive CoRoent Thoracolumbar Implants | Nu Vasive, Incorporated | 2015-06-17 | PHM |
| K151472 | 000 | NuVasive CoRoent Lumbar System | Nu Vasive, Incorporated | 2015-09-10 | MAX |
| K153419 | 000 | NuVasive CoRoent Thoracolumbar System | Nu Vasive, Incorporated | 2016-04-13 | MAX |
| K161230 | 000 | NuVasive Lumbar Interbody Implants | Nu Vasive, Incorporated | 2016-08-25 | MAX |
| K170961 | 000 | NuVasive CoRoent Small Interlock II System | Nu Vasive, Incorporated | 2017-06-08 | OVE |
| K231735 | 000 | NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody System | Nu Vasive, Incorporated | 2023-07-11 | ODP |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887517567352 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887517567352 | 00887517567352 | 887517567352 | 0887517567352 |
GMDN Terms#
| Term | Definition |
|---|---|
| Metallic spinal fusion cage, non-sterile | A non-sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae, typically due to degenerative intervertebral disks [i.e., degenerative disc disease (DDD)]. The device is typically designed as a small, hollow and/or porous, threaded or fenestrated cylinder (or other geometric form) made of metal [usually titanium (Ti)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for therapeutic spinal bone fusion to occur. Disposable devices associated with implantation may be included. This device must be sterilized prior to use. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(858)909-1800 | RA_UDI@nuvasive.com |
| +1800-475-9131 | nuvainfo@globusmedical.com |
Regulatory Flags#
- DUNS number
- 053950783
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00887517377692 | CoRoent | 6851012 | 2015-10-24 | |
| 00887517390516 | CoRoent | 6910245 | 2015-10-24 | |
| 00195377006424 | CoRoent | 6791713P2 | 6791713P2 | 2026-05-08 |
| 00195377006431 | CoRoent | 6791712P2 | 6791712P2 | 2026-05-08 |
| 00887517051905 | CoRoent | 6791715P2 | 6791715P2 | 2026-05-08 |
| 00887517051912 | CoRoent | 6791716P2 | 6791716P2 | 2026-05-08 |
| 00887517051929 | CoRoent | 6791812P2 | 6791812P2 | 2026-05-08 |
| 00887517051936 | CoRoent | 6791813P2 | 6791813P2 | 2026-05-08 |
| 00887517051943 | CoRoent | 6791814P2 | 6791814P2 | 2026-05-08 |
| 00887517051950 | CoRoent | 6791815P2 | 6791815P2 | 2026-05-08 |
| 00887517051967 | CoRoent | 6791816P2 | 6791816P2 | 2026-05-08 |
| 00887517180513 | MaXcess | 3200028 | 2022-07-20 | |
| 00887517063434 | MaXcess | 1010987 | 2019-11-21 | |
| 00887517074973 | MaXcess | 1025461 | 2019-11-21 | |
| 00887517183323 | MaXcess | 3200120 | 2019-11-21 | |
| 00887517183378 | MaXcess | 3200220 | 2019-11-21 | |
| 00887517206084 | MaXcess | 3400033 | 2019-11-21 | |
| 00887517206572 | MaXcess | 3400044 | 2019-11-21 | |
| 00887517497222 | MaXcess | 3241002 | 2019-11-21 | |
| 00887517729071 | MaXcess | 3500017 | 2019-12-04 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00197157075989 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157075996 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076009 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076016 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076023 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076030 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076047 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076054 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076061 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157075859 | ZAVATION INSERTER | Zavation LLC | MAX | 2026-05-27 |
| 00810166522366 | X-PAC | EXPANDING INNOVATIONS, INC. | MAX | 2026-05-27 |
| 00810166522373 | X-PAC | EXPANDING INNOVATIONS, INC. | MAX | 2026-05-27 |
| B70712535005S0 | Dual X Graft Tamp Short | AMPLIFY SURGICAL, INC. | MAX | 2026-05-27 |
| B707129410010130 | DUALXS T/PLIF 15 DEG x 9-12MM | AMPLIFY SURGICAL, INC. | MAX | 2026-05-27 |
| B707129410010200 | DUALXS T/PLIF 18 DEG x 10-13MM | AMPLIFY SURGICAL, INC. | MAX | 2026-05-27 |
| 07613153046196 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046202 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046202 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046219 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046219 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046226 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046233 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046233 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046288 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046295 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046301 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046301 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046318 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |
| 07613153046325 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046325 | AVS PL | Stryker Corporation | MQP | 2015-09-14 |