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AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS

Page Type
Cleared 510(K)
510(k) Number
K110419
510(k) Type
Traditional
Applicant
Stryker Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2011
Days to Decision
164 days
Submission Type
Summary

AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS

Page Type
Cleared 510(K)
510(k) Number
K110419
510(k) Type
Traditional
Applicant
Stryker Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2011
Days to Decision
164 days
Submission Type
Summary