ArthroCare Corporation
SPEEDLOCK KNOTLESS FIXATION DEVICE; 3.0MM DRILL; SHARP TIPPED OBTURATOR; LOW PROFILE DRILL GUIDDE
SKU K111044UPC MBI
In Stock
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IIFDA 510(k) Cleared (K111044)
1
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ArthroCare Corporation
Free shipping on orders over $99 · 30-day returns
SPEEDLOCK KNOTLESS FIXATION DEVICE; 3.0MM DRILL; SHARP TIPPED OBTURATOR; LOW PROFILE DRILL GUIDDE is an FDA 510(k)-cleared medical device (K111044) manufactured by ArthroCare Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 8, 2011. Regulation: 8.
