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FDA 510(k)

Assut Filbloc Permanent Sutures

K-Number: K171039 · 2017-08-29

ApplicantAssut Europe S.P.A.
Decision Date2017-08-29
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Assut Filbloc Permanent Sutures is a medical device manufactured by Assut Europe S.P.A.. It received FDA 510(k) clearance on 2017-08-29 under approval number K171039. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Assut Filbloc Permanent Sutures?

Assut Filbloc Permanent Sutures is a medical device that received FDA 510(k) clearance on 2017-08-29. It is manufactured by Assut Europe S.P.A.. The 510(k) number is K171039.

When was Assut Filbloc Permanent Sutures approved by the FDA?

Assut Filbloc Permanent Sutures received FDA 510(k) clearance on 2017-08-29, under approval number K171039.

What company makes Assut Filbloc Permanent Sutures?

Assut Filbloc Permanent Sutures is manufactured by Assut Europe S.P.A..

What is the FDA product code for Assut Filbloc Permanent Sutures?

The FDA product code for Assut Filbloc Permanent Sutures is GAW.

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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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