Clearance Summary
Fitmore Hip Stem received FDA 510(k) clearance under submission number K192236, sponsored by Zimmer GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2019-11-05.
- Submission: K192236
- Applicant / Sponsor: Zimmer GmbH
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3390
- Decision date: 2019-11-05
Classification & Regulation
This clearance is catalogued under FDA product code KWY and 21 CFR 888.3390, within the Orthopedic review panel as a Class II device.