Clearance Summary
PROstep(TM) MIS 5mm Chamfer Screw System received FDA 510(k) clearance under submission number K221645, sponsored by Wright Medical Technology. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-02-17.
- Submission: K221645
- Applicant / Sponsor: Wright Medical Technology
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2023-02-17
Classification & Regulation
This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.