
Synthes (Usa)
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SYNTHES 7.0/7.3 MM CANNULATED SCREWS is an FDA 510(k)-cleared medical device (K962011) manufactured by Synthes (Usa). 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 4, 1996. Regulation: 8.

Synthes (Usa)
SKU K100676
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SKU VM-1270020

Cardinal Health
SKU VM-1270026
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SKU VM-1270057