Stryker Spine
MODIFICATION TO STRYKER SPINE OASYS SYSTEM
SKU K062853UPC MNI
In Stock
—
IIFDA 510(k) Cleared (K062853)
1
Free shipping on orders over $99 · 30-day returns
Stryker Spine
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO STRYKER SPINE OASYS SYSTEM is an FDA 510(k)-cleared medical device (K062853) 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 23, 2006. Regulation: 8.
