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Stryker CrossFlow Integrated Arthroscopy Pump

Page Type
Cleared 510(K)
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)
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