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StentBoost Live

Page Type
Cleared 510(K)
510(k) Number
K170144
510(k) Type
Abbreviated
Applicant
Philips Medical Stystems Nederland BV
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/7/2017
Days to Decision
141 days
Submission Type
Summary

StentBoost Live

Page Type
Cleared 510(K)
510(k) Number
K170144
510(k) Type
Abbreviated
Applicant
Philips Medical Stystems Nederland BV
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/7/2017
Days to Decision
141 days
Submission Type
Summary