Musculoskeletal Clinical Regulatory Advisers
VU CPOD INTERVERTEBRAL BODU FUSION DEVICE
SKU K101363UPC ODP
In Stock
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IIFDA 510(k) Cleared (K101363)
1
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Musculoskeletal Clinical Regulatory Advisers
Free shipping on orders over $99 · 30-day returns
VU CPOD INTERVERTEBRAL BODU FUSION DEVICE is an FDA 510(k)-cleared medical device (K101363) manufactured by Musculoskeletal Clinical Regulatory Advisers. 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 15, 2010. Regulation: 8.
