DePuy Orthopaedics, Inc.
MODIFICATION TO DEPUY NEUFLEX PIP FINGER
SKU K083107UPC KYJ
In Stock
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IIFDA 510(k) Cleared (K083107)
1
Free shipping on orders over $99 · 30-day returns
DePuy Orthopaedics, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO DEPUY NEUFLEX PIP FINGER is an FDA 510(k)-cleared medical device (K083107) manufactured by DePuy Orthopaedics, 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 February 8, 2009. Regulation: 8.
