
Biomet, Inc.
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INTERLOK BIO-MODULAR HUMERAL STEMS is an FDA 510(k)-cleared medical device (K032507) manufactured by Biomet, 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 September 4, 2003. Regulation: 8.