Clearance Summary
Bodycad Unicompartmental Knee System received FDA 510(k) clearance under submission number K181302, sponsored by Bodycad Laboratories, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2019-01-17.
- Submission: K181302
- Applicant / Sponsor: Bodycad Laboratories, Inc.
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3520
- Decision date: 2019-01-17
Classification & Regulation
This clearance is catalogued under FDA product code HSX and 21 CFR 888.3520, within the Orthopedic review panel as a Class II device.