Clearance Summary
ZMR HIP SYSTEM-XL, MODELS 9921, 9922 AND 9923 received FDA 510(k) clearance under submission number K031572, sponsored by Zimmer, 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 2003-06-24.
- Submission: K031572
- Applicant / Sponsor: Zimmer, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3358
- Decision date: 2003-06-24
Classification & Regulation
This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.