Regeneration Technologies, Inc.
STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937
SKU K063584UPC HWC
In Stock
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IIFDA 510(k) Cleared (K063584)
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Free shipping on orders over $99 · 30-day returns
Regeneration Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937 is an FDA 510(k)-cleared medical device (K063584) manufactured by Regeneration Technologies, 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 May 8, 2007. Regulation: 8.
