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Stryker Consolidated Operating Room Equipment (CORE) 2 Console

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171840
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2017
Days to Decision
87 days
Submission Type
Summary

Stryker Consolidated Operating Room Equipment (CORE) 2 Console

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171840
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2017
Days to Decision
87 days
Submission Type
Summary