Name: MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE
Brand: Nuvasive, Inc.
SKU: K094054

MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K094054) manufactured by Nuvasive, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 13, 2010. Regulation: 8.

MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE

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