CoRoent 6851217
by NuVasive, LLC United States GUDID
Product code MAX
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00887517378828 | Date25 Apr 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- CoRoent
- Generic Name
- Polymeric spinal interbody fusion cage
- Model / Ref / Catalog
- 6851217
- Primary DI / UDI-DI
- 00887517378828
- 510(k) Number
- FDA Product Code
- MAX
- GMDN Term
- Polymeric spinal interbody fusion cage
- Device Class
- Class II
- Regulation Number
- 888.3080
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from NuVasive, LLC
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- Sterile: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (1)
- FDA UDI b489d824-5c83-4d19-a340-f7db1128ac27