Medical Device Manufacturer · US , Allendale , NJ

Stryker Spine - FDA 510(k) Cleared Devices

73 submissions · 72 cleared · Since 2004

73

Total

72

Cleared

0

Denied

FDA 510(k) cleared devices by Stryker Spine Neurology ✕

1 devices

1-1 of 1

Cleared Jul 28, 2011

AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS

Neurology · 164d