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FDA 510(k)

MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM

K-Number: K023388 · 2002-12-27

ApplicantMitek Worldwide
Decision Date2002-12-27
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Worldwide. It received FDA 510(k) clearance on 2002-12-27 under 510(k) number K023388. 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 MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM?

MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM is a medical device that received FDA 510(k) clearance on 2002-12-27. The listed applicant is Mitek Worldwide. The 510(k) number is K023388.

When did MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM receive FDA 510(k) clearance?

MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM received FDA 510(k) clearance on 2002-12-27, under 510(k) number K023388.

Who is the listed applicant for MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM?

The FDA 510(k) record lists Mitek Worldwide as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM?

The FDA product code for MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM is 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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