Alliance Medical Corp.
REPROCESSED EXTERNAL FIXATION DEVICE
SKU K023714UPC KTT
In Stock
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IIFDA 510(k) Cleared (K023714)
1
Free shipping on orders over $99 · 30-day returns
Alliance Medical Corp.
Free shipping on orders over $99 · 30-day returns
REPROCESSED EXTERNAL FIXATION DEVICE is an FDA 510(k)-cleared medical device (K023714) manufactured by Alliance Medical Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 2, 2003. Regulation: 8.
