Clearance Summary
ULNAR HEAD PROTHESIS received FDA 510(k) clearance under submission number K790125, sponsored by Cutter Laboratories, 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 1979-02-08.
- Submission: K790125
- Applicant / Sponsor: Cutter Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3810
- Decision date: 1979-02-08
Classification & Regulation
This clearance is catalogued under FDA product code KXE and 21 CFR 888.3810, within the Orthopedic review panel as a Class II device.