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KLS-Martin L.P.
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PATIENT CONTOURED MESH-PEEK (PCM-P) is an FDA 510(k)-cleared medical device (K072707) 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 December 18, 2007. Regulation: 8.