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FDA 510(k)

WN SYNOCTA GOLD ABUTMENT

K-Number: K063789 · 2007-05-10

ApplicantStraumann USA
Decision Date2007-05-10
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WN SYNOCTA GOLD ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Straumann USA. It received FDA 510(k) clearance on 2007-05-10 under 510(k) number K063789. 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 WN SYNOCTA GOLD ABUTMENT?

WN SYNOCTA GOLD ABUTMENT is a medical device that received FDA 510(k) clearance on 2007-05-10. The listed applicant is Straumann USA. The 510(k) number is K063789.

When did WN SYNOCTA GOLD ABUTMENT receive FDA 510(k) clearance?

WN SYNOCTA GOLD ABUTMENT received FDA 510(k) clearance on 2007-05-10, under 510(k) number K063789.

Who is the listed applicant for WN SYNOCTA GOLD ABUTMENT?

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

What is the FDA product code for WN SYNOCTA GOLD ABUTMENT?

The FDA product code for WN SYNOCTA GOLD ABUTMENT is NHA.

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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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