Clearance Summary
EIDOSMED, MODEL EDG4.0 received FDA 510(k) clearance under submission number K091992, sponsored by Eidosmed, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-12-09.
- Submission: K091992
- Applicant / Sponsor: Eidosmed, LLC
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2009-12-09
Classification & Regulation
This clearance is catalogued under FDA product code OOL and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.