Clearance Summary
MODIFICATION TO CLASSIC GREAT TOE IMPLANT received FDA 510(k) clearance under submission number K023562, sponsored by Nexa Orthopedics, 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 2002-11-13.
- Submission: K023562
- Applicant / Sponsor: Nexa Orthopedics, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3720
- Decision date: 2002-11-13
Classification & Regulation
This clearance is catalogued under FDA product code KWH and 21 CFR 888.3720, within the Orthopedic review panel as a Class II device.