Medtronic Sofamor Danek, Inc.
MODIFICATION TO TENOR SPINAL SYSTEM
SKU K022191UPC KWP
In Stock
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IIFDA 510(k) Cleared (K022191)
1
Free shipping on orders over $99 · 30-day returns
Medtronic Sofamor Danek, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO TENOR SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K022191) manufactured by Medtronic Sofamor Danek, 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 August 27, 2002. Regulation: 8.
