AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS— 510(k) K110419
Substantially EquivalentStryker Spine
FDA 510(k) clearance K110419 for AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS, Substantially Equivalent on 2011-07-28. Applicant: Stryker Spine. Device class: 2.
Clearance details
- Applicant
- Stryker Spine
- Product code
- Code GXZ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1350
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Allendale, NJ, US
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