Clearance Summary
ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY received FDA 510(k) clearance under submission number K943873, sponsored by Orthomet, 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 1995-04-26.
- Submission: K943873
- Applicant / Sponsor: Orthomet, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1995-04-26
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.