NGR — Tester, Stiffness, Cartilage, Arthroscopic Class II

FDA Device Classification

FDA product code NGR covers "Tester, Stiffness, Cartilage, Arthroscopic", a Class II medical device regulated under 21 CFR 888.1100. Submissions are reviewed by the Orthopedic panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
NGR
Device Class
Class II
Regulation Number
888.1100
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K013429osteobiologicsACTAEON PROBEJanuary 11, 2002
K010303artscan medical innovationsARTSCAN CARTILAGE STIFFNESS TESTING DEVICESeptember 11, 2001