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FDA 510(k)

IMZ MEMBRANE TACK SYSTEM

K-Number: K960945 · 1996-05-24

ApplicantInterpore Intl.
Decision Date1996-05-24
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMZ MEMBRANE TACK 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 1996-05-24 under 510(k) number K960945. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMZ MEMBRANE TACK SYSTEM?

IMZ MEMBRANE TACK SYSTEM is a medical device that received FDA 510(k) clearance on 1996-05-24. The listed applicant is Interpore Intl.. The 510(k) number is K960945.

When did IMZ MEMBRANE TACK SYSTEM receive FDA 510(k) clearance?

IMZ MEMBRANE TACK SYSTEM received FDA 510(k) clearance on 1996-05-24, under 510(k) number K960945.

Who is the listed applicant for IMZ MEMBRANE TACK 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 IMZ MEMBRANE TACK SYSTEM?

The FDA product code for IMZ MEMBRANE TACK SYSTEM is DZL.

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Related Devices (Code: DZL)

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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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