Biomet, Inc.
MODIFICATION TO: INJECTABLE MIMIX
SKU K012569UPC GXP
In Stock
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IIFDA 510(k) Cleared (K012569)
1
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Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO: INJECTABLE MIMIX is an FDA 510(k)-cleared medical device (K012569) manufactured by Biomet, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 20, 2001. Regulation: 8.
