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FDA 510(k)

TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS

K-Number: K090081 · 2010-06-22

ApplicantTalladium Espana, SL
Decision Date2010-06-22
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Talladium Espana, SL. It received FDA 510(k) clearance on 2010-06-22 under 510(k) number K090081. 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 TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS?

TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS is a medical device that received FDA 510(k) clearance on 2010-06-22. The listed applicant is Talladium Espana, SL. The 510(k) number is K090081.

When did TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS receive FDA 510(k) clearance?

TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS received FDA 510(k) clearance on 2010-06-22, under 510(k) number K090081.

Who is the listed applicant for TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS?

The FDA 510(k) record lists Talladium Espana, SL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS?

The FDA product code for TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS is NHA.

Related Clinical Trials

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Other records listing Talladium Espana, SL 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.

K221966Dynamic TiBaseK1620213.0 Dynamic TiBase

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.

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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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