Clearance Summary
KAPP CUSTOM ULNAR HEAD WRIST IMPLANT received FDA 510(k) clearance under submission number K033930, sponsored by Kapp Surgical Instrument, 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 2004-07-28.
- Submission: K033930
- Applicant / Sponsor: Kapp Surgical Instrument, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3810
- Decision date: 2004-07-28
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.