Clearance Summary
MICROAIRE SURGICAL INSTRUMENTS LLC received FDA 510(k) clearance under submission number K113128, sponsored by Microaire Surgical Instruments, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2012-08-17.
- Submission: K113128
- Applicant / Sponsor: Microaire Surgical Instruments, LLC
- Clearance pathway: Abbreviated
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.5040
- Decision date: 2012-08-17
Classification & Regulation
This clearance is catalogued under FDA product code QPB and 21 CFR 878.5040, within the General, Plastic Surgery review panel as a Class II device.