Clearance Summary
FIBULA PLATE PROLOCK WITH ANGULAR STABILITY received FDA 510(k) clearance under submission number K063672, sponsored by I.T.S. Implantat-Technologie-Systeme GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-02-02.
- Submission: K063672
- Applicant / Sponsor: I.T.S. Implantat-Technologie-Systeme GmbH
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2007-02-02
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.