Spinefrontier, Inc.
SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM
SKU K123164UPC MNH
In Stock
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IIFDA 510(k) Cleared (K123164)
1
Free shipping on orders over $99 · 30-day returns
Spinefrontier, Inc.
Free shipping on orders over $99 · 30-day returns
SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K123164) manufactured by Spinefrontier, 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 February 14, 2013. Regulation: 8.
