Nuvasive, Inc.
LAMINOPLASTY FIXATION SYSTEM
SKU K091623UPC NQW
In Stock
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IIFDA 510(k) Cleared (K091623)
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Free shipping on orders over $99 · 30-day returns
Nuvasive, Inc.
Free shipping on orders over $99 · 30-day returns
LAMINOPLASTY FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K091623) manufactured by Nuvasive, 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 October 8, 2009. Regulation: 8.
