
Seaspine, Inc.
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SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura) NanoMetalene, Cambria NanoMetalene , Vu aPOD-L NanoMetalene, Vu ePOD NanoMetalene is an FDA 510(k)-cleared medical device (K142488) manufactured by Seaspine, 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 December 17, 2014. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057