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FDA 510(k)

INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH

K-Number: K901928 · 1990-07-26

ApplicantInterpore Intl.
Decision Date1990-07-26
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1990-07-26 under 510(k) number K901928. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH?

INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Interpore Intl.. The 510(k) number is K901928.

When did INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH receive FDA 510(k) clearance?

INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH received FDA 510(k) clearance on 1990-07-26, under 510(k) number K901928.

Who is the listed applicant for INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH?

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(CASTABLE)TUB/SCRET RET RIGID ATTACH?

The FDA product code for INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH is EGG.

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Other records listing Interpore Intl. as applicant

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Related Devices (Code: EGG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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