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FDA 510(k)

Tria Firm Ureteral Stent

K-Number: K190603 · 2019-05-24

ApplicantBoston Scientific Corporation
Decision Date2019-05-24
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Tria Firm Ureteral Stent is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2019-05-24 under approval number K190603. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tria Firm Ureteral Stent?

Tria Firm Ureteral Stent is a medical device that received FDA 510(k) clearance on 2019-05-24. It is manufactured by Boston Scientific Corporation. The 510(k) number is K190603.

When was Tria Firm Ureteral Stent approved by the FDA?

Tria Firm Ureteral Stent received FDA 510(k) clearance on 2019-05-24, under approval number K190603.

What company makes Tria Firm Ureteral Stent?

Tria Firm Ureteral Stent is manufactured by Boston Scientific Corporation.

What is the FDA product code for Tria Firm Ureteral Stent?

The FDA product code for Tria Firm Ureteral Stent is FAD.

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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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