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FDA 510(k)

GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL

K-Number: K053200 · 2005-12-07

ApplicantW. L. Gore & Associates, Inc.
Decision Date2005-12-07
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 2005-12-07 under 510(k) number K053200. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL?

GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL is a medical device that received FDA 510(k) clearance on 2005-12-07. The listed applicant is W. L. Gore & Associates, Inc.. The 510(k) number is K053200.

When did GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL receive FDA 510(k) clearance?

GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL received FDA 510(k) clearance on 2005-12-07, under 510(k) number K053200.

Who is the listed applicant for GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL?

The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL?

The FDA product code for GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL is FTL.

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Other records listing W. L. Gore & Associates, Inc. as applicant

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.

K250410GORE® Tri-Lobe Balloon CatheterK240083GORE® PROPATEN® Vascular GraftK232312GORE® PROPATEN® Vascular GraftK233551GORE® ACUSEAL Vascular GraftK231505GORE® ACUSEAL Vascular GraftK222919GORE® ENFORM Biomaterial

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Related Devices (Code: FTL)

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.

K253956ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)Sofradim ProductionK253125Parietene™ Flat Sheet MeshMedtronic - Sofradim ProductionK251955Onflex™ MeshDavol Inc., Subsidiary of C. R. Bard, Inc.K251557Bard® Mesh; Bard® Mesh Pre-ShapedDavol, Inc.K250869Parietene™ Macroporous Mesh (PPM5050 )Sofradim ProductionK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedDavol, Inc.

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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