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FDA 510(k)

MAXIMUS 3.0 AND OS IMPLANTS

K-Number: K052419 · 2005-09-20

ApplicantBioHorizons Implant Systems, Inc.
Decision Date2005-09-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAXIMUS 3.0 AND OS IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is BioHorizons Implant Systems, Inc.. It received FDA 510(k) clearance on 2005-09-20 under 510(k) number K052419. 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 MAXIMUS 3.0 AND OS IMPLANTS?

MAXIMUS 3.0 AND OS IMPLANTS is a medical device that received FDA 510(k) clearance on 2005-09-20. The listed applicant is BioHorizons Implant Systems, Inc.. The 510(k) number is K052419.

When did MAXIMUS 3.0 AND OS IMPLANTS receive FDA 510(k) clearance?

MAXIMUS 3.0 AND OS IMPLANTS received FDA 510(k) clearance on 2005-09-20, under 510(k) number K052419.

Who is the listed applicant for MAXIMUS 3.0 AND OS IMPLANTS?

The FDA 510(k) record lists BioHorizons Implant Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAXIMUS 3.0 AND OS IMPLANTS?

The FDA product code for MAXIMUS 3.0 AND OS IMPLANTS is DZE.

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Other records listing BioHorizons Implant Systems, Inc. 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.

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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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