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FDA 510(k)

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS

K-Number: K870331 · 1987-03-02

ApplicantInterpore Intl.
Decision Date1987-03-02
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1987-03-02 under 510(k) number K870331. 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 IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS?

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS is a medical device that received FDA 510(k) clearance on 1987-03-02. The listed applicant is Interpore Intl.. The 510(k) number is K870331.

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

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS received FDA 510(k) clearance on 1987-03-02, under 510(k) number K870331.

Who is the listed applicant for IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS?

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 IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS?

The FDA product code for IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS is EGG.

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Related Devices (Code: EGG)

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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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