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FDA 510(k)

INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER

K-Number: K922732 · 1994-02-10

ApplicantInterpore Intl.
Decision Date1994-02-10
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1994-02-10 under 510(k) number K922732. 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 CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER?

INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Interpore Intl.. The 510(k) number is K922732.

When did INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER receive FDA 510(k) clearance?

INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER received FDA 510(k) clearance on 1994-02-10, under 510(k) number K922732.

Who is the listed applicant for INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER?

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 CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER?

The FDA product code for INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER is DZE.

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Other records listing Interpore Intl. as applicant

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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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