Depuy Spine, A Johnson & Johnson Company
MODIFICATION TO VERTEBROPLASTIC RADIOPAQUE BONE CEMENT
SKU K071927UPC NDN
In Stock
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IIFDA 510(k) Cleared (K071927)
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Free shipping on orders over $99 · 30-day returns
Depuy Spine, A Johnson & Johnson Company
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO VERTEBROPLASTIC RADIOPAQUE BONE CEMENT is an FDA 510(k)-cleared medical device (K071927) manufactured by Depuy Spine, A Johnson & Johnson Company. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 2007. Regulation: 8.
