
Spine Wave, Inc.
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Sniper (R) Spine System is an FDA 510(k)-cleared medical device (K160003) 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 25, 2016. Regulation: 8.

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SKU K100676
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