Arcos Modular Revision System 31-301123
Arcos Modular Revision System 31-301123 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K100469 on 7 Dec 2010 and listed in FDA GUDID since 28 Oct 2016 (UDI-DI 00880304490147), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00880304490147 | Date28 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK100469 | Date7 Dec 2010 | StatusActive |
Official records
- AccessGUDID record 00880304490147
- FDA 510(k) database K100469
Across registries
- FDA 510(k) K100469 decided 7 Dec 2010 Active
- FDA GUDID UDI-DI 00880304490147 listed 28 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K100469
- Listed FDA GUDID 00880304490147
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Arcos Modular Revision System
- Generic name
- Femoral stem prosthesis trial
- Model / Ref / Catalog
- 31-301123
- Primary DI / UDI-DI
- 00880304490147
- 510(k) Number
- FDA product code
- MAY, MEH, KWZ, JDI, LPH, LZO, KWY
- GMDN term
- Femoral stem prosthesis trial
- Device class
- Class II
- Regulation number
- 888.3353, 888.3310, 888.3350, 888.3358, 888.3390
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Femoral stem prosthesis trial.