Clearance Summary
REMUSK MP received FDA 510(k) clearance under submission number K922029, sponsored by Equipement Biomedical Specialise, 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 1992-10-06.
- Submission: K922029
- Applicant / Sponsor: Equipement Biomedical Specialise, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.1240
- Decision date: 1992-10-06
Classification & Regulation
This clearance is catalogued under FDA product code LBB and 21 CFR 888.1240, within the Orthopedic review panel as a Class II device.