FDA 510(k)

ENDOANCHOR AND OPENANCHOR

K-Number: K013749 · 2002-02-11

Decision Date2002-02-11

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ENDOANCHOR AND OPENANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 2002-02-11 under 510(k) number K013749. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOANCHOR AND OPENANCHOR?

ENDOANCHOR AND OPENANCHOR is a medical device that received FDA 510(k) clearance on 2002-02-11. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K013749.

When did ENDOANCHOR AND OPENANCHOR receive FDA 510(k) clearance?

ENDOANCHOR AND OPENANCHOR received FDA 510(k) clearance on 2002-02-11, under 510(k) number K013749.

Who is the listed applicant for ENDOANCHOR AND OPENANCHOR?

The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOANCHOR AND OPENANCHOR?

The FDA product code for ENDOANCHOR AND OPENANCHOR is GDW.

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Other records listing Ethicon Endo-Surgery, Inc. as applicant

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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.