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FDA 510(k)

StentBoost Live

K-Number: K170144 · 2017-06-07

ApplicantPhilips Medical Stystems Nederland BV
Decision Date2017-06-07
Product CodeOWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

StentBoost Live is a medical device manufactured by Philips Medical Stystems Nederland BV. It received FDA 510(k) clearance on 2017-06-07 under approval number K170144. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the StentBoost Live?

StentBoost Live is a medical device that received FDA 510(k) clearance on 2017-06-07. It is manufactured by Philips Medical Stystems Nederland BV. The 510(k) number is K170144.

When was StentBoost Live approved by the FDA?

StentBoost Live received FDA 510(k) clearance on 2017-06-07, under approval number K170144.

What company makes StentBoost Live?

StentBoost Live is manufactured by Philips Medical Stystems Nederland BV.

What is the FDA product code for StentBoost Live?

The FDA product code for StentBoost Live is OWB.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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