Clearance Summary
MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM received FDA 510(k) clearance under submission number K990603, sponsored by Danek Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-03-10.
- Submission: K990603
- Applicant / Sponsor: Danek Medical, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 1999-03-10
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.