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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223918
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland B.V.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223918
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/8/2023
Days to Decision
161 days
Submission Type
Summary