Clearance Summary
ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD received FDA 510(k) clearance under submission number K993873, sponsored by Alphatec Mfg., 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 2000-01-03.
- Submission: K993873
- Applicant / Sponsor: Alphatec Mfg., Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2000-01-03
Classification & Regulation
This clearance is catalogued under FDA product code KTT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.