JARVIS Glenoid Rerverse Shoulder Prosthesis
by Fournitures Hospitalieres Industrie 40 variants
Listed
Valid until
Not applicable
FDA recalls
None foundDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03661489722219 | Date18 Jul 2025 | StatusListed |
Recalls
No FDA recalls found in the data synced 8 Jun 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / Reference
- 272221 - JARVIS OPEN GUIDE WIRE 10° WEAR ROUND BASEPLATE
- Primary DI / UDI-DI
- 03661489722219
- 510(k) Number
- FDA Product Code
- KWS, KWT, PHX
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device Class
- Class II
- Regulation Number
- 888.3660, 888.3650
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Fournitures Hospitalieres Industrie
Properties
Other properties (12)
- 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