Clearance Summary
PTI STERNAL CLOSURE WIRE SUTURE received FDA 510(k) clearance under submission number K910067, sponsored by Pioneering Technologies, 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 1991-05-06.
- Submission: K910067
- Applicant / Sponsor: Pioneering Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4495
- Decision date: 1991-05-06
Classification & Regulation
This clearance is catalogued under FDA product code GAQ and 21 CFR 878.4495, within the General, Plastic Surgery review panel as a Class II device.