Clearance Summary
TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG received FDA 510(k) clearance under submission number K810193, sponsored by Ace Orthopedic Manufacturing Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1981-03-20.
- Submission: K810193
- Applicant / Sponsor: Ace Orthopedic Manufacturing Co.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5960
- Decision date: 1981-03-20
Classification & Regulation
This clearance is catalogued under FDA product code HAX and 21 CFR 882.5960, within the Neurology review panel as a Class II device.