
Biopro, Inc.
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BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685 is an FDA 510(k)-cleared medical device (K083490) manufactured by Biopro, 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 March 17, 2009. Regulation: 8.