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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 the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2017-11-03 under 510(k) 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. The listed applicant is Boston Scientific Corporation. The 510(k) number is K172060.

When did Capio SLIM Suture Capturing Device receive FDA 510(k) clearance?

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

Who is the listed applicant for Capio SLIM Suture Capturing Device?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

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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Related Devices (Code: PWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K173527Digitex Delivery DeviceColoplast A/S

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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