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FDA 510(k)

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS

K-Number: K863680 · 1986-10-24

ApplicantInterpore Intl.
Decision Date1986-10-24
Product CodeDZE
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 1986-10-24 under 510(k) number K863680. 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 IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS?

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is Interpore Intl.. The 510(k) number is K863680.

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 1986-10-24, under 510(k) number K863680.

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 DZE.

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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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