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FDA 510(k)

MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT

K-Number: K914041 · 1991-12-09

ApplicantMidwest Implant Sales, Inc.
Decision Date1991-12-09
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Implant Sales, Inc.. It received FDA 510(k) clearance on 1991-12-09 under 510(k) number K914041. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT?

MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT is a medical device that received FDA 510(k) clearance on 1991-12-09. The listed applicant is Midwest Implant Sales, Inc.. The 510(k) number is K914041.

When did MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT receive FDA 510(k) clearance?

MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT received FDA 510(k) clearance on 1991-12-09, under 510(k) number K914041.

Who is the listed applicant for MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT?

The FDA 510(k) record lists Midwest Implant Sales, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT?

The FDA product code for MIDWEST IMPLANT HEXED 3.3 MM CYLINDER TYPE IMPLANT is DZE.

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Other records listing Midwest Implant Sales, Inc. 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.

K914042MIDWEST IMPLANT HEXED 3.75MM SELF TAPPING IMPLANTK914043MIDWEST IMPLANT HEXED 3.75MM STANDARD THREAD IMPLA

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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