Globus Medical, Inc.
RELIEVE LAMINOPLASTY FIXATION SYSTEM
SKU K080664UPC NQW
In Stock
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IIFDA 510(k) Cleared (K080664)
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Free shipping on orders over $99 · 30-day returns
Globus Medical, Inc.
Free shipping on orders over $99 · 30-day returns
RELIEVE LAMINOPLASTY FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K080664) manufactured by Globus Medical, 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 July 24, 2008. Regulation: 8.
