Medtronic Spine, LLC
KYPHON ANCHOR FACET SCREW SYSTEM
SKU K101765UPC MRW
In Stock
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FDA 510(k) Cleared (K101765)
1
Free shipping on orders over $99 · 30-day returns
Medtronic Spine, LLC
Free shipping on orders over $99 · 30-day returns
KYPHON ANCHOR FACET SCREW SYSTEM is an FDA 510(k)-cleared medical device (K101765) manufactured by Medtronic Spine, LLC. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on October 21, 2010.
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