Clearance Summary
PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM received FDA 510(k) clearance under submission number K073177, sponsored by Pioneer Surgical Technology. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-05-13.
- Submission: K073177
- Applicant / Sponsor: Pioneer Surgical Technology
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2008-05-13
Classification & Regulation
This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.