Nuvasive, Inc.
MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM
SKU K070273UPC KWQ
In Stock
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IIFDA 510(k) Cleared (K070273)
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Free shipping on orders over $99 · 30-day returns
Nuvasive, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM is an FDA 510(k)-cleared medical device (K070273) 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 April 2, 2007. Regulation: 8.
