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PercuNav Image Fusion and Interventional Navigation

Page Type
Cleared 510(K)
510(k) Number
K201053
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2020
Days to Decision
23 days
Submission Type
Summary

PercuNav Image Fusion and Interventional Navigation

Page Type
Cleared 510(K)
510(k) Number
K201053
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2020
Days to Decision
23 days
Submission Type
Summary