4900-45-50
by Zimmer, Inc.
4900-45-50 (00-4900-045-50) is a Class II device made by Zimmer, Inc., cleared under FDA 510(k) K140508 on 14 Aug 2014 and listed in FDA GUDID since 9 Oct 2015 (UDI-DI 00889024076433), 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 | Number00889024076433 | Date9 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK140508 | Date14 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00889024076433
- FDA 510(k) database K140508
Across registries
- FDA 510(k) K140508 decided 14 Aug 2014 Active
- FDA GUDID UDI-DI 00889024076433 listed 9 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K140508
- Listed FDA GUDID 00889024076433
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Implantable bone nut
- Model / Ref / Catalog
- 4900-45-50, 00-4900-045-50
- Primary DI / UDI-DI
- 00889024076433
- 510(k) Number
- FDA product code
- JDI
- GMDN term
- Implantable bone nut
- Device class
- Class II
- Regulation number
- 888.3350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Implantable bone nut.