Exactech Sterile Modular Drill Bit
510(k) K960720
Exactech Sterile Modular Drill Bit is a Class I device made by Exactech, Inc., cleared under FDA 510(k) K960720 on 23 Apr 1996, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK960720 | Date23 Apr 1996 | StatusActive |
Official records
- FDA 510(k) database K960720
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HWE
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4820
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code HWE (Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment).
- XFO112001 by Stryker GmbH
- HHI ELECTRIC CONSOLE #875-000 by H&H Instruments
- EZX XTL40A by IMEDICOM CO., LTD.
- Shrill® JSHPP8000 by Joimax GmbH
- 899710033 89971.0033 by Richard Wolf GmbH
- ACETABULAR REAMER EVO 2 DRAGGER D61 mm H0037556199 by HPF SRL
- VERTEBRIS 899751304 by Richard Wolf GmbH
- 2410-21 00-2410-021-00 by Zimmer, Inc.
- ACETABULAR REAMER EVO 2 Ti CUP D42 mm H0038554299 by HPF SRL
- EZX Blade XTB400 by IMEDICOM CO., LTD.