Humeris Shoulder 902-4805
by Fx Solutions
Humeris Shoulder 902-4805 is a Class II device made by Fx Solutions, cleared under FDA 510(k) K163669 on 17 May 2017 and listed in FDA GUDID since 22 May 2017 (UDI-DI 03701037304310), active (FDA 510(k)), not in commercial distribution (GUDID) as of 22 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 | Number03701037304310 | Date22 May 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK163669 | Date17 May 2017 | StatusActive |
Official records
- AccessGUDID record 03701037304310
- FDA 510(k) database K163669
Across registries
- FDA 510(k) K163669 decided 17 May 2017 Active
- FDA GUDID UDI-DI 03701037304310 listed 22 May 2017 Listed
Timeline
- Cleared FDA 510(k) K163669
- Listed FDA GUDID 03701037304310
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Humeris Shoulder
- Generic name
- Orthopaedic surgical procedure kit, non-medicated, reusable
- Model / Ref / Catalog
- 902-4805
- Primary DI / UDI-DI
- 03701037304310
- 510(k) Number
- FDA product code
- HSD
- GMDN term
- Orthopaedic surgical procedure kit, non-medicated, reusable
- Device class
- Class II
- Regulation number
- 888.3690
- GUDID distribution status
- Not in Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Orthopaedic surgical procedure kit, non-medicated, reusable.