Clearance Summary
STRYKER KNIFELIGHT received FDA 510(k) clearance under submission number K961122, sponsored by Stryker Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1996-08-22.
- Submission: K961122
- Applicant / Sponsor: Stryker Instruments
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4580
- Decision date: 1996-08-22
Classification & Regulation
This clearance is catalogued under FDA product code FTD and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.