Clearance Summary
DISPOSABLE ARTHROSCOPY CANNULA SET received FDA 510(k) clearance under submission number K813000, sponsored by Clinical Technology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1982-01-22.
- Submission: K813000
- Applicant / Sponsor: Clinical Technology Corp.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1982-01-22
Classification & Regulation
This clearance is catalogued under FDA product code LXH and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.