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FDA 510(k)

MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL

K-Number: K070084 · 2007-03-08

ApplicantEst. Anthogyr
Decision Date2007-03-08
Product CodeEFA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Est. Anthogyr. It received FDA 510(k) clearance on 2007-03-08 under 510(k) number K070084. The device is classified under product code EFA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL?

MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL is a medical device that received FDA 510(k) clearance on 2007-03-08. The listed applicant is Est. Anthogyr. The 510(k) number is K070084.

When did MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL receive FDA 510(k) clearance?

MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL received FDA 510(k) clearance on 2007-03-08, under 510(k) number K070084.

Who is the listed applicant for MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL?

The FDA 510(k) record lists Est. Anthogyr as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL?

The FDA product code for MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL is EFA.

Related Clinical Trials

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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Other records listing Est. Anthogyr 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.

K060317ANTHOGYR CONTRA ANGLES AND HANDPIECESK020431FIBIOCORE

Related Devices (Code: EFA)

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.

K192809Dental HandpieceMicro-Nx Co., Ltd.K163239SMARTmaticKaltenbach & Voigt GmbHK101172RDT3 HANDPIECE HEAD MODEL RDT3Redent Nova, Ltd.K093894ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLEAnthogyrK092446INTRA LUX HEAD 3 LDSYKaltenbach & Voigt GmbH & Co.K090055LOW & HIGH SPEED KITDpm USA Corp.

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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