
C.R. Bard, Inc.
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BARD COLLAMEND IMPLANT, MODELS 1175102, 1175103, 1175104, 1175105, 1175106 is an FDA 510(k)-cleared medical device (K063178) manufactured by C.R. Bard, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 2006. Regulation: 8.