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FDA 510(k)

IDT-1104 IMPLANT (SCREW-IN-THREADED)

K-Number: K903046 · 1991-04-19

ApplicantMinimatic Implant Technology
Decision Date1991-04-19
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IDT-1104 IMPLANT (SCREW-IN-THREADED) 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 1991-04-19 under 510(k) number K903046. 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 IDT-1104 IMPLANT (SCREW-IN-THREADED)?

IDT-1104 IMPLANT (SCREW-IN-THREADED) is a medical device that received FDA 510(k) clearance on 1991-04-19. The listed applicant is Minimatic Implant Technology. The 510(k) number is K903046.

When did IDT-1104 IMPLANT (SCREW-IN-THREADED) receive FDA 510(k) clearance?

IDT-1104 IMPLANT (SCREW-IN-THREADED) received FDA 510(k) clearance on 1991-04-19, under 510(k) number K903046.

Who is the listed applicant for IDT-1104 IMPLANT (SCREW-IN-THREADED)?

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 IDT-1104 IMPLANT (SCREW-IN-THREADED)?

The FDA product code for IDT-1104 IMPLANT (SCREW-IN-THREADED) 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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