EIDOSMED, MODEL EDG4.0— 510(k) K091992
Substantially EquivalentEidosmed, LLC
FDA 510(k) clearance K091992 for EIDOSMED, MODEL EDG4.0, Substantially Equivalent on 2009-12-09. Applicant: Eidosmed, LLC. Device class: 2.
Clearance details
- Applicant
- Eidosmed, LLC
- Product code
- Code OOL
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Deerfield, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.