Clearance Summary
SAW BLADE received FDA 510(k) clearance under submission number K933298, sponsored by Omega Surgical Instruments, Inc.. 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 1993-08-09.
- Submission: K933298
- Applicant / Sponsor: Omega Surgical Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1993-08-09
Classification & Regulation
This clearance is catalogued under FDA product code GFA and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.