Spineology, Inc.
K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM
SKU K002371UPC KWQ
In Stock
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IIFDA 510(k) Cleared (K002371)
1
Free shipping on orders over $99 · 30-day returns
Spineology, Inc.
Free shipping on orders over $99 · 30-day returns
K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K002371) manufactured by Spineology, 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 September 14, 2000. Regulation: 8.
