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FDA 510(k)

Assut Filbloc Permanent Sutures

K-Number: K171039 · 2017-08-29

Decision Date2017-08-29
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Assut Filbloc Permanent Sutures is the device name listed in this FDA 510(k) record. The listed applicant is Assut Europe S.P.A.. It received FDA 510(k) clearance on 2017-08-29 under 510(k) 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. The listed applicant is Assut Europe S.P.A.. The 510(k) number is K171039.

When did Assut Filbloc Permanent Sutures receive FDA 510(k) clearance?

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

Who is the listed applicant for Assut Filbloc Permanent Sutures?

The FDA 510(k) record lists Assut Europe S.P.A. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: GAW)

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.

Official Source

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