Juggerstitch™ 110025571
Juggerstitch™ 110025571 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K150424 on 15 May 2015 and listed in FDA GUDID since 16 Mar 2017 (UDI-DI 00880304806825), 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 | Number00880304806825 | Date16 Mar 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK150424 | Date15 May 2015 | StatusActive |
Official records
- AccessGUDID record 00880304806825
- FDA 510(k) database K150424
Across registries
- FDA 510(k) K150424 decided 15 May 2015 Active
- FDA GUDID UDI-DI 00880304806825 listed 16 Mar 2017 Listed
Timeline
- Cleared FDA 510(k) K150424
- Listed FDA GUDID 00880304806825
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Juggerstitch™
- Generic name
- Soft-tissue/mesh anchor, non-bioabsorbable
- Model / Ref / Catalog
- 110025571
- Primary DI / UDI-DI
- 00880304806825
- 510(k) Number
- FDA product code
- MBI
- GMDN term
- Soft-tissue/mesh anchor, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Soft-tissue/mesh anchor, non-bioabsorbable.