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FDA 510(k)

PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR

K-Number: K063273 · 2006-11-22

ApplicantDepuy Miltek, A Johnson & Johnson Co.
Decision Date2006-11-22
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Miltek, A Johnson & Johnson Co.. It received FDA 510(k) clearance on 2006-11-22 under 510(k) number K063273. 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 PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR?

PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR is a medical device that received FDA 510(k) clearance on 2006-11-22. The listed applicant is Depuy Miltek, A Johnson & Johnson Co.. The 510(k) number is K063273.

When did PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR receive FDA 510(k) clearance?

PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR received FDA 510(k) clearance on 2006-11-22, under 510(k) number K063273.

Who is the listed applicant for PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR?

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

What is the FDA product code for PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR?

The FDA product code for PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR 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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