Clearance Summary
MODIFIED ZICKEL INTRAMEDULLARY ROD SYSTEM received FDA 510(k) clearance under submission number K926213, sponsored by Osteo Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1993-06-17.
- Submission: K926213
- Applicant / Sponsor: Osteo Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3020
- Decision date: 1993-06-17
Classification & Regulation
This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.