
DePuy Orthopaedics, Inc.
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DEPUY 1 GENTAMICIN BONE CEMENT is an FDA 510(k)-cleared medical device (K023103) manufactured by DePuy Orthopaedics, 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 28, 2003. Regulation: 8.