Clearance Summary
PIONEER MAXFUSE VERTEBRAL BODY REPLACEMENT DEVICE received FDA 510(k) clearance under submission number K131724, sponsored by Pioneer Surgical 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 2013-12-24.
- Submission: K131724
- Applicant / Sponsor: Pioneer Surgical Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2013-12-24
Classification & Regulation
This clearance is catalogued under FDA product code MQP and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.