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FDA 510(k)

MINISCREWS ANCHORING SYSTEM, M.A.S.

K-Number: K062367 · 2006-12-08

ApplicantMicerium S.P.A.
Decision Date2006-12-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINISCREWS ANCHORING SYSTEM, M.A.S. is the device name listed in this FDA 510(k) record. The listed applicant is Micerium S.P.A.. It received FDA 510(k) clearance on 2006-12-08 under 510(k) number K062367. 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 MINISCREWS ANCHORING SYSTEM, M.A.S.?

MINISCREWS ANCHORING SYSTEM, M.A.S. is a medical device that received FDA 510(k) clearance on 2006-12-08. The listed applicant is Micerium S.P.A.. The 510(k) number is K062367.

When did MINISCREWS ANCHORING SYSTEM, M.A.S. receive FDA 510(k) clearance?

MINISCREWS ANCHORING SYSTEM, M.A.S. received FDA 510(k) clearance on 2006-12-08, under 510(k) number K062367.

Who is the listed applicant for MINISCREWS ANCHORING SYSTEM, M.A.S.?

The FDA 510(k) record lists Micerium S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINISCREWS ANCHORING SYSTEM, M.A.S.?

The FDA product code for MINISCREWS ANCHORING SYSTEM, M.A.S. is DZE.

Related Clinical Trials

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Other records listing Micerium S.P.A. 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.

K103474ENA TEMP AND ENAMEL PLUS TEMP (TWO DIFFERENT PROPRIETARY NAMES FOR THE SAME PRODUCT)K072978TENDER ORTHO BOND-ENA BOND-ENA ETCHK063170TENDER FIBERK062355ENA CEMK062906ENA HFO COMPOSITE SYSTEM

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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