Clearance Summary
CONQUEST FN received FDA 510(k) clearance under submission number K172785, sponsored by Smith & Nephew. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-12-22.
- Submission: K172785
- Applicant / Sponsor: Smith & Nephew
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2017-12-22
Classification & Regulation
This clearance is catalogued under FDA product code JDO and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.