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FDA 510(k)

A-1101 CAST ABUTMENT

K-Number: K903039 · 1990-12-26

ApplicantMinimatic Implant Technology
Decision Date1990-12-26
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

A-1101 CAST ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Minimatic Implant Technology. It received FDA 510(k) clearance on 1990-12-26 under 510(k) number K903039. 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 A-1101 CAST ABUTMENT?

A-1101 CAST ABUTMENT is a medical device that received FDA 510(k) clearance on 1990-12-26. The listed applicant is Minimatic Implant Technology. The 510(k) number is K903039.

When did A-1101 CAST ABUTMENT receive FDA 510(k) clearance?

A-1101 CAST ABUTMENT received FDA 510(k) clearance on 1990-12-26, under 510(k) number K903039.

Who is the listed applicant for A-1101 CAST ABUTMENT?

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

What is the FDA product code for A-1101 CAST ABUTMENT?

The FDA product code for A-1101 CAST ABUTMENT is DZE.

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Other records listing Minimatic Implant Technology 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.

K911776DPI-1106 IMPLANT, MODIFICATIONK903515HH-1119 HEALING HEADK911112DEVICE PART NUMBERS: - 1400 SERIESK905039IMPLANT, THREADED EXTERNAL HEX, TAPERED SHOULDERK904707BC 1208 IMPLANT, THREADED EXTERNAL HEXK903043ICT-1108 IMPLANT- THREADED (CEMENT TYPE ABUTMENT)

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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

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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