
Valley Forge Scientific Corp.
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MALIS SURGICAL MESH FOR SKULL /SPINAL COLUMN REPAI is an FDA 510(k)-cleared medical device (K861822) manufactured by Valley Forge Scientific Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 10, 1986. Regulation: 8.

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