ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE— 510(k) K010303
Substantially EquivalentArtscan Medical Innovations
FDA 510(k) clearance K010303 for ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE, Substantially Equivalent on 2001-09-11. Applicant: Artscan Medical Innovations.
Clearance details
- Applicant
- Artscan Medical Innovations
- Product code
- Code NGR
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Akron, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.