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FDA 510(k)

ABUTMENT - COMPLETE

K-Number: K974280 · 1998-02-20

ApplicantThe Implant Center of the Palm Beaches
Decision Date1998-02-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ABUTMENT - COMPLETE is the device name listed in this FDA 510(k) record. The listed applicant is The Implant Center of the Palm Beaches. It received FDA 510(k) clearance on 1998-02-20 under 510(k) number K974280. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABUTMENT - COMPLETE?

ABUTMENT - COMPLETE is a medical device that received FDA 510(k) clearance on 1998-02-20. The listed applicant is The Implant Center of the Palm Beaches. The 510(k) number is K974280.

When did ABUTMENT - COMPLETE receive FDA 510(k) clearance?

ABUTMENT - COMPLETE received FDA 510(k) clearance on 1998-02-20, under 510(k) number K974280.

Who is the listed applicant for ABUTMENT - COMPLETE?

The FDA 510(k) record lists The Implant Center of the Palm Beaches as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABUTMENT - COMPLETE?

The FDA product code for ABUTMENT - COMPLETE is DZE.

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Other records listing The Implant Center of the Palm Beaches 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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