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FDA 510(k)

MITEK MINI ANCHOR

K-Number: K992623 · 1999-11-02

ApplicantMitek Products
Decision Date1999-11-02
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MITEK MINI ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Mitek Products. It received FDA 510(k) clearance on 1999-11-02 under 510(k) number K992623. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MITEK MINI ANCHOR?

MITEK MINI ANCHOR is a medical device that received FDA 510(k) clearance on 1999-11-02. The listed applicant is Mitek Products. The 510(k) number is K992623.

When did MITEK MINI ANCHOR receive FDA 510(k) clearance?

MITEK MINI ANCHOR received FDA 510(k) clearance on 1999-11-02, under 510(k) number K992623.

Who is the listed applicant for MITEK MINI ANCHOR?

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

What is the FDA product code for MITEK MINI ANCHOR?

The FDA product code for MITEK MINI ANCHOR is DZL.

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Other records listing Mitek Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K013572MITEK BIOCRYL INTERFERENCE SCREWSK013781RIDIDFIX 2.7MM BTB CROSS PIN KITK002639BIOKNOTLESS ANCHORK010633RIGIDFIX SOFT TISSUE ACL CROSSPIN SYSTEMK002406MITEK 2GII MENISCAL REPAIR SYSTEMK003076MITEK CUFFTACK

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Related Devices (Code: DZL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254286Guided Bone Regeneration SystemDentalMaster(Xiamen)Medical Technology Co., Ltd.K250123Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)Hager& Meisinger GmbHK251569Bone ScrewOsstem Implant Co., Ltd.K243190USTOMED Bone Fixation/Bone Augmentation Systems - PINUstomed Instrumente Ulrich Storz GmbH & Co. KGK233419GBR SystemProimtech Saglik Urunleri Anonim SirketiK240321MP Pin flat without thread (36BMP000020/MP20)Hager& Meisinger GmbH

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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