Stryker Knifelight
510(k) K100884
Stryker Knifelight is a Class II device made by Howmedica Osteonics Corp., cleared under FDA 510(k) K100884 on 25 Jun 2010, 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 | NumberK100884 | Date25 Jun 2010 | StatusActive |
Official records
- FDA 510(k) database K100884
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- FTD
- Device class
- Class II
- Regulation
- 21 CFR Part 878.4580
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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