Clearance Summary
TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500 received FDA 510(k) clearance under submission number K092482, sponsored by Shippert Medical Technologies Corp.. 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 2009-12-04.
- Submission: K092482
- Applicant / Sponsor: Shippert Medical Technologies Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.5040
- Decision date: 2009-12-04
Classification & Regulation
This clearance is catalogued under FDA product code MUU and 21 CFR 878.5040, within the General, Plastic Surgery review panel as a Class II device.