CoRoent
- Primary DI
- 00887517329998
- Brand
- CoRoent
- Company
- Nuvasive, Inc.
- Model
- 6791015
- Device description
- CoRoent® SI Ta Markers, 15x17x14 7° Con
- 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#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K102547 | 000 | COROENT INTERLOCK SYSTEM | Nuvasive, Inc. | 2011-02-07 | OVE |
| K142299 | 000 | CoRoent Small Interlock System | Nu Vasive, Incorporated | 2014-11-25 | OVE |
| K161442 | 000 | NuVasive® CoRoent® Small Interlock™ System | Nu Vasive, Incorporated | 2016-09-28 | OVE |
| K170961 | 000 | NuVasive CoRoent Small Interlock II System | Nu Vasive, Incorporated | 2017-06-08 | OVE |
| K192582 | 000 | NuVasive CoRoent Small Interlock System | Nu Vasive, Incorporated | 2019-11-13 | 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 |
|---|---|---|---|---|
| 00887517329998 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887517329998 | 00887517329998 | 887517329998 | 0887517329998 |
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#
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|---|---|---|---|---|
| 00887517127693 | MaXcess | 7070422 | 7070422 | 2026-07-27 |
| 00887517065100 | ACP | 18008223 | 18008223 | 2026-04-25 |
| 00887517065124 | ACP | 18008312 | 18008312 | 2026-04-25 |
| 00887517065162 | ACP | 18008316 | 18008316 | 2026-04-25 |
| 00887517065186 | ACP | 18008318 | 18008318 | 2026-04-25 |
| 00887517065384 | ACP | 18008512 | 18008512 | 2026-04-25 |
| 00887517065612 | ACP | 18008622 | 18008622 | 2026-04-25 |
| 00887517065643 | ACP | 18009117 | 18009117 | 2026-04-25 |
| 00887517065667 | ACP | 18009119 | 18009119 | 2026-04-25 |
| 00887517065681 | ACP | 18009121 | 18009121 | 2026-04-25 |
| 00887517065926 | ACP | 18009229 | 18009229 | 2026-04-25 |
| 00887517100412 | VuePoint | 8977115 | 8977115 | 2026-04-25 |
| 00887517156297 | ReLine | 11010511 | 11010511 | 2026-04-25 |
| 00887517156822 | ReLine | 11010530 | 11010530 | 2026-04-25 |
| 00887517378828 | CoRoent | 6851217 | 6851217 | 2026-04-25 |
| 00887517413673 | MAS PLIF | 7070042 | 7070042 | 2026-04-25 |
| 00887517645135 | CoRoent | 6800508 | 6800508 | 2026-04-25 |
| 00887517645142 | CoRoent | 6800510 | 6800510 | 2026-04-25 |
| 00887517645166 | CoRoent | 6800514 | 6800514 | 2026-04-25 |
| 00887517645173 | CoRoent | 6801508 | 6801508 | 2026-04-25 |
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