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FDA 510(k)

ORTHO ANCHOR SCREWS

K-Number: K073461 · 2008-01-25

ApplicantMis Implants Technologies , Ltd.
Decision Date2008-01-25
Product CodeOAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORTHO ANCHOR SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Mis Implants Technologies , Ltd.. It received FDA 510(k) clearance on 2008-01-25 under 510(k) number K073461. The device is classified under product code OAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHO ANCHOR SCREWS?

ORTHO ANCHOR SCREWS is a medical device that received FDA 510(k) clearance on 2008-01-25. The listed applicant is Mis Implants Technologies , Ltd.. The 510(k) number is K073461.

When did ORTHO ANCHOR SCREWS receive FDA 510(k) clearance?

ORTHO ANCHOR SCREWS received FDA 510(k) clearance on 2008-01-25, under 510(k) number K073461.

Who is the listed applicant for ORTHO ANCHOR SCREWS?

The FDA 510(k) record lists Mis Implants Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHO ANCHOR SCREWS?

The FDA product code for ORTHO ANCHOR SCREWS is OAT.

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Other records listing Mis Implants Technologies , Ltd. 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.

K182228MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentsK180282MIS Internal Hex Dental Implant SystemK173326MIS CONNECT Conical Connection AbutmentK172505MIS C1 Narrow Platform Conical Connection Implant System, MIS C1 Wide Platform Conical Connection AbutmentsK163349MIS V3 Conical Connection Dental Implant System­K112162CONICAL CONNECTION IMPLANTS

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Related Devices (Code: OAT)

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.

K260268OrthoEasy Pal; OrthoEasy Pal Long NeckBernhard Förster GmbH (Bernhard Foerster Ltd.)K242944Leone Orthodontic Implant TAD (Temporary Anchorage Device)Leone S.P.A.K231502Mini ScrewsProimtech Saglik Urunleri Anonim SirketiK231913T-FITTechwin Co., Ltd.K222245ACR Screw SystemBiomaterials Korea, Inc.K202163Mico One Orthodontic ScrewZe Fang Technology Co., Ltd.

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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