Interpore Cross Intl.
MODIFICATION TO ALTIUS OCT SYSTEM
SKU K043229UPC KWP
In Stock
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IIFDA 510(k) Cleared (K043229)
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Free shipping on orders over $99 · 30-day returns
Interpore Cross Intl.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO ALTIUS OCT SYSTEM is an FDA 510(k)-cleared medical device (K043229) manufactured by Interpore Cross Intl.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 20, 2004. Regulation: 8.
