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FDA 510(k)

GC AADVA BO AC ABUTMENTS

K-Number: K103234 · 2011-06-30

ApplicantGC America, Inc.
Decision Date2011-06-30
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GC AADVA BO AC ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is GC America, Inc.. It received FDA 510(k) clearance on 2011-06-30 under 510(k) number K103234. 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 GC AADVA BO AC ABUTMENTS?

GC AADVA BO AC ABUTMENTS is a medical device that received FDA 510(k) clearance on 2011-06-30. The listed applicant is GC America, Inc.. The 510(k) number is K103234.

When did GC AADVA BO AC ABUTMENTS receive FDA 510(k) clearance?

GC AADVA BO AC ABUTMENTS received FDA 510(k) clearance on 2011-06-30, under 510(k) number K103234.

Who is the listed applicant for GC AADVA BO AC ABUTMENTS?

The FDA 510(k) record lists GC America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GC AADVA BO AC ABUTMENTS?

The FDA product code for GC AADVA BO AC ABUTMENTS is NHA.

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Other records listing GC America, Inc. as applicant

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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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