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AltaTrack Equipment R1.2, AltaTrack Guidewire, AltaTrack 3D Hub

Page Type
Cleared 510(K)
510(k) Number
K223918
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland BV
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/8/2023
Days to Decision
161 days
Submission Type
Summary

AltaTrack Equipment R1.2, AltaTrack Guidewire, AltaTrack 3D Hub

Page Type
Cleared 510(K)
510(k) Number
K223918
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland BV
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/8/2023
Days to Decision
161 days
Submission Type
Summary