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FDA 510(k)

ELATION MB METAL REINFORCED PLASTIC BRACKET

K-Number: K092030 · 2009-07-24

ApplicantDentsply Interntional
Decision Date2009-07-24
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELATION MB METAL REINFORCED PLASTIC BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Interntional. It received FDA 510(k) clearance on 2009-07-24 under 510(k) number K092030. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELATION MB METAL REINFORCED PLASTIC BRACKET?

ELATION MB METAL REINFORCED PLASTIC BRACKET is a medical device that received FDA 510(k) clearance on 2009-07-24. The listed applicant is Dentsply Interntional. The 510(k) number is K092030.

When did ELATION MB METAL REINFORCED PLASTIC BRACKET receive FDA 510(k) clearance?

ELATION MB METAL REINFORCED PLASTIC BRACKET received FDA 510(k) clearance on 2009-07-24, under 510(k) number K092030.

Who is the listed applicant for ELATION MB METAL REINFORCED PLASTIC BRACKET?

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

What is the FDA product code for ELATION MB METAL REINFORCED PLASTIC BRACKET?

The FDA product code for ELATION MB METAL REINFORCED PLASTIC BRACKET is DYW.

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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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