Seaspine, Inc.
INTEGRA LAMINOPLASTY SYSTEM
SKU K130830UPC NQW
In Stock
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IIFDA 510(k) Cleared (K130830)
1
Free shipping on orders over $99 · 30-day returns
Seaspine, Inc.
Free shipping on orders over $99 · 30-day returns
INTEGRA LAMINOPLASTY SYSTEM is an FDA 510(k)-cleared medical device (K130830) manufactured by Seaspine, 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 May 8, 2013. Regulation: 8.
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