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FDA 510(k)

Capio SLIM Suture Capturing Device

K-Number: K172060 · 2017-11-03

ApplicantBoston Scientific Corporation
Decision Date2017-11-03
Product CodePWI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Capio SLIM Suture Capturing Device is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2017-11-03 under approval number K172060. The device is classified under product code PWI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Capio SLIM Suture Capturing Device?

Capio SLIM Suture Capturing Device is a medical device that received FDA 510(k) clearance on 2017-11-03. It is manufactured by Boston Scientific Corporation. The 510(k) number is K172060.

When was Capio SLIM Suture Capturing Device approved by the FDA?

Capio SLIM Suture Capturing Device received FDA 510(k) clearance on 2017-11-03, under approval number K172060.

What company makes Capio SLIM Suture Capturing Device?

Capio SLIM Suture Capturing Device is manufactured by Boston Scientific Corporation.

What is the FDA product code for Capio SLIM Suture Capturing Device?

The FDA product code for Capio SLIM Suture Capturing Device is PWI.

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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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