Wrightmedicaltechnologyinc
ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE
SKU K092201UPC JWH
In Stock
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IIFDA 510(k) Cleared (K092201)
1
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Wrightmedicaltechnologyinc
Free shipping on orders over $99 · 30-day returns
ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE is an FDA 510(k)-cleared medical device (K092201) manufactured by Wrightmedicaltechnologyinc. 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 19, 2009. Regulation: 8.
