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FDA 510(k)

NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS

K-Number: K122602 · 2013-03-13

ApplicantNobel Biocare AB
Decision Date2013-03-13
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare AB. It received FDA 510(k) clearance on 2013-03-13 under 510(k) number K122602. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS?

NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS is a medical device that received FDA 510(k) clearance on 2013-03-13. The listed applicant is Nobel Biocare AB. The 510(k) number is K122602.

When did NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS receive FDA 510(k) clearance?

NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS received FDA 510(k) clearance on 2013-03-13, under 510(k) number K122602.

Who is the listed applicant for NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS?

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

What is the FDA product code for NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS?

The FDA product code for NOBELPROCERA TI ABUTMENT CAMLOG PLATFORMS is NHA.

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Other records listing Nobel Biocare AB 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.

K253988LiteSet TraysK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewK252197Nobel Biocare S Series ImplantsK243834NobelZygoma TiUltra Implant systemK240346NobelProcera Zirconia Implant BridgeK233208NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium

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Related Devices (Code: NHA)

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.

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLCK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, 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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