Taperloc Complete 51-201170
Taperloc Complete 51-201170 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K120030 on 17 Aug 2012 and listed in FDA GUDID since 22 Sep 2016 (UDI-DI 00880304480940), 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 | Number00880304480940 | Date22 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK120030 | Date17 Aug 2012 | StatusActive |
Official records
- AccessGUDID record 00880304480940
- FDA 510(k) database K120030
Across registries
- FDA 510(k) K120030 decided 17 Aug 2012 Active
- FDA GUDID UDI-DI 00880304480940 listed 22 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K120030
- Listed FDA GUDID 00880304480940
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Taperloc Complete
- Generic name
- Bone file/rasp, manual, reusable
- Model / Ref / Catalog
- 51-201170
- Primary DI / UDI-DI
- 00880304480940
- 510(k) Number
- FDA product code
- LZO, LPH, KWY, JDI, OQG, MEH, KWL, KWZ
- GMDN term
- Bone file/rasp, manual, reusable
- Device class
- Class II
- Regulation number
- 888.3353, 888.3358, 888.3390, 888.3350, 888.3360, 888.3310
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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