Last synced on 14 November 2025 at 11:06 pm

AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter

Page Type
Cleared 510(K)
510(k) Number
K201081
510(k) Type
Traditional
Applicant
Philips Medical System Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
239 days
Submission Type
Summary

AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter

Page Type
Cleared 510(K)
510(k) Number
K201081
510(k) Type
Traditional
Applicant
Philips Medical System Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
12/17/2020
Days to Decision
239 days
Submission Type
Summary