
Arthrosurface, Inc.
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CAP 7.0MM MTP RESURFACING HEMI-ARTHROPLASTY is an FDA 510(k)-cleared medical device (K063370) manufactured by Arthrosurface, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2007. Regulation: 8.