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Stryker CrossFlow Integrated Arthroscopy Pump

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191259
510(k) Type
Traditional
Applicant
Stryker Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2019
Days to Decision
63 days
Submission Type
Summary

Stryker CrossFlow Integrated Arthroscopy Pump

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191259
510(k) Type
Traditional
Applicant
Stryker Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2019
Days to Decision
63 days
Submission Type
Summary