Clearance Summary
SPIRAL RADIUS RODDING SYSTEM received FDA 510(k) clearance under submission number K000009, sponsored by United States Surgical, A Division of Tyco Healthc. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-03-10.
- Submission: K000009
- Applicant / Sponsor: United States Surgical, A Division of Tyco Healthc
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2000-03-10
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.