
Laurimed, LLC
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LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002 is an FDA 510(k)-cleared medical device (K082194) manufactured by Laurimed, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 2008. Regulation: 8.