Stryker S2 Drill
510(k) K141935
Stryker S2 Drill is a Class II device made by Stryker Corporation, cleared under FDA 510(k) K141935 on 26 Sep 2014, 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 | NumberK141935 | Date26 Sep 2014 | StatusActive |
Official records
- FDA 510(k) database K141935
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ERL
- Device class
- Class II
- Regulation
- 21 CFR Part 874.4250
- Advisory committee
- Ear, Nose, Throat
- FDA decision
- SESE Substantially Equivalent
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