Stryker Spine
MODIFICATION TO OASYS SYSTEM
SKU K072568UPC KWP
In Stock
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IIFDA 510(k) Cleared (K072568)
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Free shipping on orders over $99 · 30-day returns
Stryker Spine
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO OASYS SYSTEM is an FDA 510(k)-cleared medical device (K072568) manufactured by Stryker Spine. 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 4, 2007. Regulation: 8.
