
Medtronic Sofamor Danek
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MODIFICATION TO VERTE-STACK SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K041197) manufactured by Medtronic Sofamor Danek. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 8, 2004. Regulation: 8.