Ortho Kinematics, Inc.
VMA System version 3.0
SKU K172327UPC LLZ
In Stock
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IIFDA 510(k) Cleared (K172327)
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Free shipping on orders over $99 · 30-day returns
Ortho Kinematics, Inc.
Free shipping on orders over $99 · 30-day returns
VMA System version 3.0 is an FDA 510(k)-cleared medical device (K172327) manufactured by Ortho Kinematics, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 24, 2017. Regulation: 8.
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