
Vesitec Medical, Inc.
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BONE ANCHOR FOR SOFT TISSUE ATTACHMENT is an FDA 510(k)-cleared medical device (K932925) manufactured by Vesitec Medical, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 25, 1994. Regulation: 8.

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