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FDA 510(k)

PROCERA ALLCERAM BRIDGE MATERIAL

K-Number: K020269 · 2002-03-27

ApplicantProcera Sandvik AB
Decision Date2002-03-27
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROCERA ALLCERAM BRIDGE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Procera Sandvik AB. It received FDA 510(k) clearance on 2002-03-27 under 510(k) number K020269. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCERA ALLCERAM BRIDGE MATERIAL?

PROCERA ALLCERAM BRIDGE MATERIAL is a medical device that received FDA 510(k) clearance on 2002-03-27. The listed applicant is Procera Sandvik AB. The 510(k) number is K020269.

When did PROCERA ALLCERAM BRIDGE MATERIAL receive FDA 510(k) clearance?

PROCERA ALLCERAM BRIDGE MATERIAL received FDA 510(k) clearance on 2002-03-27, under 510(k) number K020269.

Who is the listed applicant for PROCERA ALLCERAM BRIDGE MATERIAL?

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

What is the FDA product code for PROCERA ALLCERAM BRIDGE MATERIAL?

The FDA product code for PROCERA ALLCERAM BRIDGE MATERIAL is EIH.

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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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