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FDA 510(k)

CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor

K-Number: K172666 · 2017-12-01

ApplicantSutureease, Inc.
Decision Date2017-12-01
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor is a medical device manufactured by Sutureease, Inc.. It received FDA 510(k) clearance on 2017-12-01 under approval number K172666. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor?

CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor is a medical device that received FDA 510(k) clearance on 2017-12-01. It is manufactured by Sutureease, Inc.. The 510(k) number is K172666.

When was CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor approved by the FDA?

CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor received FDA 510(k) clearance on 2017-12-01, under approval number K172666.

What company makes CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor?

CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor is manufactured by Sutureease, Inc..

What is the FDA product code for CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor?

The FDA product code for CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor is OCW.

Related Clinical Trials

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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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