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AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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