Clearance Summary
APEX KIRSCHNER WIRES AND STEINMANN PINS received FDA 510(k) clearance under submission number K112254, sponsored by Apex Tools & Orthopedics Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-10-11.
- Submission: K112254
- Applicant / Sponsor: Apex Tools & Orthopedics Co.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2011-10-11
Classification & Regulation
This clearance is catalogued under FDA product code HTY and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.