Clearance Summary
WAGNER SL REVISION STEM LATERAL received FDA 510(k) clearance under submission number K043356, sponsored by Zimmer Austin, 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 2005-04-18.
- Submission: K043356
- Applicant / Sponsor: Zimmer Austin, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3353
- Decision date: 2005-04-18
Classification & Regulation
This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.