Clearance Summary
K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM) received FDA 510(k) clearance under submission number K023770, sponsored by Kinetikos Medical, 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 2002-12-12.
- Submission: K023770
- Applicant / Sponsor: Kinetikos Medical, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3730
- Decision date: 2002-12-12
Classification & Regulation
This clearance is catalogued under FDA product code KWD and 21 CFR 888.3730, within the Orthopedic review panel as a Class II device.