Interpore Cross Intl.
INTERPORE CROSS CEMENT RESTRICTOR
SKU K023908UPC JDK
In Stock
—
IIFDA 510(k) Cleared (K023908)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Interpore Cross Intl.
Free shipping on orders over $99 · 30-day returns
INTERPORE CROSS CEMENT RESTRICTOR is an FDA 510(k)-cleared medical device (K023908) manufactured by Interpore Cross Intl.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 15, 2003. Regulation: 8.
