Juggerknot 110025794
Juggerknot 110025794 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K150768 on 4 Sep 2015 and listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00880304701229), 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 | Number00880304701229 | Date28 Jul 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK150768 | Date4 Sep 2015 | StatusActive |
Official records
- AccessGUDID record 00880304701229
- FDA 510(k) database K150768
Across registries
- FDA 510(k) K150768 decided 4 Sep 2015 Active
- FDA GUDID UDI-DI 00880304701229 listed 28 Jul 2017 Listed
Timeline
- Cleared FDA 510(k) K150768
- Listed FDA GUDID 00880304701229
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Juggerknot
- Generic name
- Surgical drill guide, single-use
- Model / Ref / Catalog
- 110025794
- Primary DI / UDI-DI
- 00880304701229
- 510(k) Number
- FDA product code
- MBI
- GMDN term
- Surgical drill guide, single-use
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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