
KLS-Martin L.P.
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PATIENT CONTOURED MESH (PCM) is an FDA 510(k)-cleared medical device (K062570) manufactured by KLS-Martin L.P.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 2006. Regulation: 8.