FDA 510(k)

BARD SACROCOLPOPEXY GRAFT

K-Number: K090739 · 2009-11-10

Decision Date2009-11-10

Product CodeOTO

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BARD SACROCOLPOPEXY GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2009-11-10 under 510(k) number K090739. The device is classified under product code OTO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD SACROCOLPOPEXY GRAFT?

BARD SACROCOLPOPEXY GRAFT is a medical device that received FDA 510(k) clearance on 2009-11-10. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K090739.

When did BARD SACROCOLPOPEXY GRAFT receive FDA 510(k) clearance?

BARD SACROCOLPOPEXY GRAFT received FDA 510(k) clearance on 2009-11-10, under 510(k) number K090739.

Who is the listed applicant for BARD SACROCOLPOPEXY GRAFT?

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

What is the FDA product code for BARD SACROCOLPOPEXY GRAFT?

The FDA product code for BARD SACROCOLPOPEXY GRAFT is OTO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.