Clearance Summary
EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD received FDA 510(k) clearance under submission number K890162, sponsored by Dhason Brothers, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1989-02-13.
- Submission: K890162
- Applicant / Sponsor: Dhason Brothers, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1989-02-13
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.