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FDA 510(k)

SPI EASY DENTAL IMPLANT ABUTMENT

K-Number: K023645 · 2002-11-13

Decision Date2002-11-13
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPI EASY DENTAL IMPLANT ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Thommen Medical AG. It received FDA 510(k) clearance on 2002-11-13 under 510(k) number K023645. 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 SPI EASY DENTAL IMPLANT ABUTMENT?

SPI EASY DENTAL IMPLANT ABUTMENT is a medical device that received FDA 510(k) clearance on 2002-11-13. The listed applicant is Thommen Medical AG. The 510(k) number is K023645.

When did SPI EASY DENTAL IMPLANT ABUTMENT receive FDA 510(k) clearance?

SPI EASY DENTAL IMPLANT ABUTMENT received FDA 510(k) clearance on 2002-11-13, under 510(k) number K023645.

Who is the listed applicant for SPI EASY DENTAL IMPLANT ABUTMENT?

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

What is the FDA product code for SPI EASY DENTAL IMPLANT ABUTMENT?

The FDA product code for SPI EASY DENTAL IMPLANT ABUTMENT is NHA.

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.

Other records listing Thommen Medical AG 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.

View all 26 devices →

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.

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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