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FDA 510(k)

INTERPORE IMZ CYLINDER IMPLANT SYSTEM

K-Number: K913228 · 1992-10-13

ApplicantInterpore Intl.
Decision Date1992-10-13
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE IMZ CYLINDER IMPLANT 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 1992-10-13 under 510(k) number K913228. 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 CYLINDER IMPLANT SYSTEM?

INTERPORE IMZ CYLINDER IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Interpore Intl.. The 510(k) number is K913228.

When did INTERPORE IMZ CYLINDER IMPLANT SYSTEM receive FDA 510(k) clearance?

INTERPORE IMZ CYLINDER IMPLANT SYSTEM received FDA 510(k) clearance on 1992-10-13, under 510(k) number K913228.

Who is the listed applicant for INTERPORE IMZ CYLINDER IMPLANT 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 CYLINDER IMPLANT SYSTEM?

The FDA product code for INTERPORE IMZ CYLINDER IMPLANT SYSTEM is DZE.

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Other records listing Interpore Intl. as applicant

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Related Devices (Code: 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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