Cohort Medical Products Group, Inc.
BONE SCREW
SKU K943804UPC HWC
In Stock
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IIFDA 510(k) Cleared (K943804)
1
Free shipping on orders over $99 · 30-day returns
Cohort Medical Products Group, Inc.
Free shipping on orders over $99 · 30-day returns
BONE SCREW is an FDA 510(k)-cleared medical device (K943804) manufactured by Cohort Medical Products Group, 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 December 7, 1994. Regulation: 8.
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