Dextera MicroCutter 30 Blue Reload, Dextera MicroCutter 30 Curved Tip Blue Reload, Dextera MicroCutter 30 White Reload, Dextera MicroCutter 30 Curved Tip White Reload
by Dextera Surgical, Inc. 510(k)
Active
510(k) K171561
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK171561 | Date28 Aug 2017 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- GDW
- Device Class
- Class II
- Regulation
- 21 CFR Part 878.4750
- Advisory Committee
- General, Plastic Surgery
- FDA Decision
- SESE Substantially Equivalent