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MultiGen™ 2 RF Generator System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170242
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2017
Days to Decision
119 days
Submission Type
Summary

MultiGen™ 2 RF Generator System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170242
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2017
Days to Decision
119 days
Submission Type
Summary