Clearance Summary
TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER received FDA 510(k) clearance under submission number K922308, sponsored by Ti-Mesh, 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 1993-01-12.
- Submission: K922308
- Applicant / Sponsor: Ti-Mesh, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 1993-01-12
Classification & Regulation
This clearance is catalogued under FDA product code FTM and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.