Clearance Summary
TAMARACK ANTERIOR THORACOLUNBAR received FDA 510(k) clearance under submission number K050390, sponsored by Alphatec/Nexmed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-03-14.
- Submission: K050390
- Applicant / Sponsor: Alphatec/Nexmed
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2005-03-14
Classification & Regulation
This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.