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FDA 510(k)

BIOKNOTLESS AND LUPINE PLUS ANCHORS

K-Number: K062170 · 2006-08-22

ApplicantDepuy Mitek, A Johnson & Johnson Company
Decision Date2006-08-22
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOKNOTLESS AND LUPINE PLUS ANCHORS 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 2006-08-22 under 510(k) number K062170. 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 BIOKNOTLESS AND LUPINE PLUS ANCHORS?

BIOKNOTLESS AND LUPINE PLUS ANCHORS is a medical device that received FDA 510(k) clearance on 2006-08-22. The listed applicant is Depuy Mitek, A Johnson & Johnson Company. The 510(k) number is K062170.

When did BIOKNOTLESS AND LUPINE PLUS ANCHORS receive FDA 510(k) clearance?

BIOKNOTLESS AND LUPINE PLUS ANCHORS received FDA 510(k) clearance on 2006-08-22, under 510(k) number K062170.

Who is the listed applicant for BIOKNOTLESS AND LUPINE PLUS ANCHORS?

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 BIOKNOTLESS AND LUPINE PLUS ANCHORS?

The FDA product code for BIOKNOTLESS AND LUPINE PLUS ANCHORS is JDR.

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Other records listing Depuy Mitek, A Johnson & Johnson Company as applicant

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Related Devices (Code: JDR)

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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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