Alliance Medical, Inc.
REPROCESSED EXTERNAL FIXATION DEVICE
SKU K012634UPC KTW
In Stock
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IIFDA 510(k) Cleared (K012634)
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Free shipping on orders over $99 · 30-day returns
Alliance Medical, Inc.
Free shipping on orders over $99 · 30-day returns
REPROCESSED EXTERNAL FIXATION DEVICE is an FDA 510(k)-cleared medical device (K012634) manufactured by Alliance Medical, 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 23, 2002. Regulation: 8.
