Interventional Spine, Inc.
Opticage Expandable Interbody Fusion Device
SKU K152156UPC MAX
In Stock
—
IIFDA 510(k) Cleared (K152156)
1
Free shipping on orders over $99 · 30-day returns
Interventional Spine, Inc.
Free shipping on orders over $99 · 30-day returns
Opticage Expandable Interbody Fusion Device is an FDA 510(k)-cleared medical device (K152156) manufactured by Interventional Spine, 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 October 18, 2015. Regulation: 8.
Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020
Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057