Clearance Summary
BONE GRAFT WASHER, MODEL 9090114 - 9090118 received FDA 510(k) clearance under submission number K994122, sponsored by Danek Medical, 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 2000-02-18.
- Submission: K994122
- Applicant / Sponsor: Danek Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2000-02-18
Classification & Regulation
This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.