Aesculap, Inc.
MODIFICATION TO S4 SPINAL SYSTEM
SKU K060152UPC MNI
In Stock
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IIFDA 510(k) Cleared (K060152)
1
Free shipping on orders over $99 · 30-day returns
Aesculap, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO S4 SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K060152) manufactured by Aesculap, 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 February 2, 2006. Regulation: 8.
