Spine Wave, Inc.
MODIFICATION TO STAXX FX SYSTEM
SKU K063606UPC OBL
In Stock
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IIFDA 510(k) Cleared (K063606)
1
Free shipping on orders over $99 · 30-day returns
Spine Wave, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO STAXX FX SYSTEM is an FDA 510(k)-cleared medical device (K063606) manufactured by Spine Wave, 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 12, 2007. Regulation: 8.
