Clearance Summary
INTERMEDICS ORTHOPEDICS REAMERS received FDA 510(k) clearance under submission number K931733, sponsored by Intermedics Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1994-01-26.
- Submission: K931733
- Applicant / Sponsor: Intermedics Orthopedics
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1994-01-26
Classification & Regulation
This clearance is catalogued under FDA product code HTP and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.