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FDA 510(k)

INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM

K-Number: K900793 · 1990-07-27

ApplicantInterpore Intl.
Decision Date1990-07-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K900793. 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 INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM?

INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Interpore Intl.. The 510(k) number is K900793.

When did INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM receive FDA 510(k) clearance?

INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM received FDA 510(k) clearance on 1990-07-27, under 510(k) number K900793.

Who is the listed applicant for INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM?

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

What is the FDA product code for INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM?

The FDA product code for INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM is DZE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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