Clearance Summary
MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX received FDA 510(k) clearance under submission number K030460, sponsored by Brennen Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-03-07.
- Submission: K030460
- Applicant / Sponsor: Brennen Medical, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2003-03-07
Classification & Regulation
This clearance is catalogued under FDA product code PAG and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.