Baxter Healthcare Corp
ACL DRILL GUIDE SYSTEM
SKU K892655UPC LXI
In Stock
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IFDA 510(k) Cleared (K892655)
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Free shipping on orders over $99 · 30-day returns
Baxter Healthcare Corp
Free shipping on orders over $99 · 30-day returns
ACL DRILL GUIDE SYSTEM is an FDA 510(k)-cleared medical device (K892655) manufactured by Baxter Healthcare Corp. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 27, 1989. Regulation: 8.
