
Depuy Miltek, A Johnson & Johnson Co.
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PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR is an FDA 510(k)-cleared medical device (K063273) manufactured by Depuy Miltek, A Johnson & Johnson Co.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 21, 2006. Regulation: 8.