Us Spine
MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM
SKU K081883UPC MNH
In Stock
—
IIFDA 510(k) Cleared (K081883)
1
Free shipping on orders over $99 · 30-day returns
Us Spine
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K081883) manufactured by Us 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 September 23, 2008. Regulation: 8.
