ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE— 510(k) K010303

Name: FDA 510(k) clearance K010303
Creator: U.S. Food and Drug Administration
Published: 2001-09-11

Substantially Equivalent

Artscan Medical Innovations

FDA 510(k) clearance K010303 for ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE, Substantially Equivalent on 2001-09-11. Applicant: Artscan Medical Innovations. Device class: 2.

Clearance details

Applicant: Artscan Medical Innovations
Product code: Code NGR
Device class: Class 2
Regulation: 21 CFR 888.1100
Advisory panel: Orthopedic
Date received: 2000-12-05
Decision date: 2001-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, US

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