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PercuNav Image Fusion and Interventional Navigation

Page Type
Cleared 510(K)
510(k) Number
K170716
510(k) Type
Traditional
Applicant
Philips Ultrasound Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2017
Days to Decision
43 days
Submission Type
Summary

PercuNav Image Fusion and Interventional Navigation

Page Type
Cleared 510(K)
510(k) Number
K170716
510(k) Type
Traditional
Applicant
Philips Ultrasound Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2017
Days to Decision
43 days
Submission Type
Summary