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FDA 510(k)

MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD

K-Number: K071257 · 2007-06-29

ApplicantDepuy Mitek, A Johnson & Johnson Company
Decision Date2007-06-29
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Mitek, A Johnson & Johnson Company. It received FDA 510(k) clearance on 2007-06-29 under 510(k) number K071257. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD?

MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD is a medical device that received FDA 510(k) clearance on 2007-06-29. The listed applicant is Depuy Mitek, A Johnson & Johnson Company. The 510(k) number is K071257.

When did MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD receive FDA 510(k) clearance?

MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD received FDA 510(k) clearance on 2007-06-29, under 510(k) number K071257.

Who is the listed applicant for MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD?

The FDA 510(k) record lists Depuy Mitek, A Johnson & Johnson Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD?

The FDA product code for MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD is JDR.

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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.

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