24-3001
24-3001 is a Class II device made by Biomet Microfixation, Inc, cleared under FDA 510(k) K082293 on 9 Sep 2008 and listed in FDA GUDID since 18 Nov 2016 (UDI-DI 00841036135010), 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 | Number00841036135010 | Date18 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082293 | Date9 Sep 2008 | StatusActive |
Official records
- AccessGUDID record 00841036135010
- FDA 510(k) database K082293
Across registries
- FDA 510(k) K082293 decided 9 Sep 2008 Active
- FDA GUDID UDI-DI 00841036135010 listed 18 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K082293
- Listed FDA GUDID 00841036135010
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Endoscopic video imaging system
- Model / Ref / Catalog
- 24-3001
- Primary DI / UDI-DI
- 00841036135010
- 510(k) Number
- FDA product code
- GCJ, HRX
- GMDN term
- Endoscopic video imaging system
- Device class
- Class II
- Regulation number
- 876.1500, 888.1100
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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