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FDA 510(k)

MULTILINK HYBRID ABUTMENT CEMENT

K-Number: K130436 · 2013-08-20

ApplicantIvoclar Vivadent, AG
Decision Date2013-08-20
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MULTILINK HYBRID ABUTMENT CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, AG. It received FDA 510(k) clearance on 2013-08-20 under 510(k) number K130436. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTILINK HYBRID ABUTMENT CEMENT?

MULTILINK HYBRID ABUTMENT CEMENT is a medical device that received FDA 510(k) clearance on 2013-08-20. The listed applicant is Ivoclar Vivadent, AG. The 510(k) number is K130436.

When did MULTILINK HYBRID ABUTMENT CEMENT receive FDA 510(k) clearance?

MULTILINK HYBRID ABUTMENT CEMENT received FDA 510(k) clearance on 2013-08-20, under 510(k) number K130436.

Who is the listed applicant for MULTILINK HYBRID ABUTMENT CEMENT?

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

What is the FDA product code for MULTILINK HYBRID ABUTMENT CEMENT?

The FDA product code for MULTILINK HYBRID ABUTMENT CEMENT is EMA.

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Related Devices (Code: EMA)

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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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