CoRoent 6801512
by NuVasive, LLC United States GUDID
Product code MAX
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00887517645197 | Date25 Apr 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- CoRoent
- Generic Name
- Spinal implant trial
- Model / Ref / Catalog
- 6801512
- Primary DI / UDI-DI
- 00887517645197
- 510(k) Number
- FDA Product Code
- MAX, MQP
- GMDN Term
- Spinal implant trial
- Device Class
- Class II
- Regulation Number
- 888.3080, 888.3060
- 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 (13)
- Sterile: No
- Single Use: No
- Implantable: 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 d4deaa71-ce67-488d-8a4e-18461de342ba