Clearance Summary
DYNAMOMETER - MODEL FCE AND MODEL MSC received FDA 510(k) clearance under submission number K042889, sponsored by Ametek. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-11-16.
- Submission: K042889
- Applicant / Sponsor: Ametek
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.1240
- Decision date: 2004-11-16
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.