Clearance Summary
SPIRAL RADIUS 90-D SST SYSTEM received FDA 510(k) clearance under submission number K012273, sponsored by United States Surgical, A Division of Tyco Healthc. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-08-15.
- Submission: K012273
- Applicant / Sponsor: United States Surgical, A Division of Tyco Healthc
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2001-08-15
Classification & Regulation
This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.