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FDA 510(k)

VENTRALIGHT ST MESH

K-Number: K101851 · 2010-07-15

ApplicantDavol Inc., Sub. C. R. Bard, Inc.
Decision Date2010-07-15
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VENTRALIGHT ST MESH is the device name listed in this FDA 510(k) record. The listed applicant is Davol Inc., Sub. C. R. Bard, Inc.. It received FDA 510(k) clearance on 2010-07-15 under 510(k) number K101851. 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 VENTRALIGHT ST MESH?

VENTRALIGHT ST MESH is a medical device that received FDA 510(k) clearance on 2010-07-15. The listed applicant is Davol Inc., Sub. C. R. Bard, Inc.. The 510(k) number is K101851.

When did VENTRALIGHT ST MESH receive FDA 510(k) clearance?

VENTRALIGHT ST MESH received FDA 510(k) clearance on 2010-07-15, under 510(k) number K101851.

Who is the listed applicant for VENTRALIGHT ST MESH?

The FDA 510(k) record lists Davol Inc., Sub. C. R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTRALIGHT ST MESH?

The FDA product code for VENTRALIGHT ST MESH is FTL.

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Other records listing Davol Inc., Sub. C. R. Bard, 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.

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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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