
Depuy Spine, Inc.
Free shipping on orders over $99 · 30-day returns
PIPELINE II ACCESS SYSTEM is an FDA 510(k)-cleared medical device (K062814) manufactured by Depuy Spine, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 14, 2006. Regulation: 8.