Clearance Summary
MITEK GII ANCHOR received FDA 510(k) clearance under submission number K953877, sponsored by Mitek Surgical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1995-12-29.
- Submission: K953877
- Applicant / Sponsor: Mitek Surgical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 1995-12-29
Classification & Regulation
This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.