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FDA 510(k)

AA-1110 ANALOG ABUTMENT

K-Number: K903042 · 1990-11-13

ApplicantMinimatic Implant Technology
Decision Date1990-11-13
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AA-1110 ANALOG 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 1990-11-13 under 510(k) number K903042. 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 AA-1110 ANALOG ABUTMENT?

AA-1110 ANALOG ABUTMENT is a medical device that received FDA 510(k) clearance on 1990-11-13. The listed applicant is Minimatic Implant Technology. The 510(k) number is K903042.

When did AA-1110 ANALOG ABUTMENT receive FDA 510(k) clearance?

AA-1110 ANALOG ABUTMENT received FDA 510(k) clearance on 1990-11-13, under 510(k) number K903042.

Who is the listed applicant for AA-1110 ANALOG 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 AA-1110 ANALOG ABUTMENT?

The FDA product code for AA-1110 ANALOG 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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