Sterilmed, Inc.
REPROCESSED EXTERNAL FIXATION DEVICE
SKU K083636UPC KTT
In Stock
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IIFDA 510(k) Cleared (K083636)
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Free shipping on orders over $99 · 30-day returns
Sterilmed, Inc.
Free shipping on orders over $99 · 30-day returns
REPROCESSED EXTERNAL FIXATION DEVICE is an FDA 510(k)-cleared medical device (K083636) manufactured by Sterilmed, 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 March 1, 2009. Regulation: 8.
