Genesys Spine
TILOCK PEDICLE SCREW SYSTEM
SKU K100757UPC NKB
In Stock
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IIFDA 510(k) Cleared (K100757)
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Free shipping on orders over $99 · 30-day returns
Genesys Spine
Free shipping on orders over $99 · 30-day returns
TILOCK PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K100757) manufactured by Genesys Spine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 30, 2010. Regulation: 8.
