Clearance Summary
TIGR Matrix Surgical Mesh, TIGR Surgical Mesh received FDA 510(k) clearance under submission number K191749, sponsored by Novus Scientific AB. 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 2020-03-26.
- Submission: K191749
- Applicant / Sponsor: Novus Scientific AB
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2020-03-26
Classification & Regulation
This clearance is catalogued under FDA product code OWT and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.