Clearance Summary
ANCHORMAN Tibial Ligament Fixation Device received FDA 510(k) clearance under submission number K170388, sponsored by Summit Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-07-25.
- Submission: K170388
- Applicant / Sponsor: Summit Medical , Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2017-07-25
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.