Clearance Summary
SYNTHES VA LCP ANKLE TRAUMA SYSTEM received FDA 510(k) clearance under submission number K120854, sponsored by Synthes USA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-06-18.
- Submission: K120854
- Applicant / Sponsor: Synthes USA
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2012-06-18
Classification & Regulation
This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.