Clearance Summary
TELOS DISTAL TARGETING DEVICE received FDA 510(k) clearance under submission number K880381, sponsored by Austin Assoc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1988-03-15.
- Submission: K880381
- Applicant / Sponsor: Austin Assoc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1988-03-15
Classification & Regulation
This clearance is catalogued under FDA product code HXY and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.