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FDA 510(k)

INTERPORE THREADED IMPLANT

K-Number: K960371 · 1996-03-08

ApplicantInterpore Intl.
Decision Date1996-03-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE THREADED IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1996-03-08 under 510(k) number K960371. 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 THREADED IMPLANT?

INTERPORE THREADED IMPLANT is a medical device that received FDA 510(k) clearance on 1996-03-08. The listed applicant is Interpore Intl.. The 510(k) number is K960371.

When did INTERPORE THREADED IMPLANT receive FDA 510(k) clearance?

INTERPORE THREADED IMPLANT received FDA 510(k) clearance on 1996-03-08, under 510(k) number K960371.

Who is the listed applicant for INTERPORE THREADED IMPLANT?

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 THREADED IMPLANT?

The FDA product code for INTERPORE THREADED IMPLANT is DZE.

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Other records listing Interpore Intl. as applicant

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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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