Spine Wave, Inc.
Proficient Posterior Cervical Spine System
SKU K162639UPC NKG
In Stock
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IIFDA 510(k) Cleared (K162639)
1
Free shipping on orders over $99 · 30-day returns
Spine Wave, Inc.
Free shipping on orders over $99 · 30-day returns
Proficient Posterior Cervical Spine System is an FDA 510(k)-cleared medical device (K162639) manufactured by Spine Wave, 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 February 6, 2017. Regulation: 8.
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