Biomet, Inc.
TunneLoc Tibial Fixation Device
SKU K193092UPC MBI
In Stock
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IIFDA 510(k) Cleared (K193092)
1
Free shipping on orders over $99 · 30-day returns
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
TunneLoc Tibial Fixation Device is an FDA 510(k)-cleared medical device (K193092) manufactured by Biomet, 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 January 1, 2020. Regulation: 8.
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