Vertebron, Inc.
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
SKU K071376UPC NKB
In Stock
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IIFDA 510(k) Cleared (K071376)
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Free shipping on orders over $99 · 30-day returns
Vertebron, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K071376) manufactured by Vertebron, 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 June 12, 2007. Regulation: 8.
