
Interpore Cross Intl.
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SYNERGY VLS CAP NUT MODELS 2206, 6102 is an FDA 510(k)-cleared medical device (K000236) manufactured by Interpore Cross Intl.. 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 15, 2000. Regulation: 8.