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FDA 510(k)

INTERPORE 200 POROUS HYDROXYAPATITE

K-Number: K852975 · 1985-10-31

ApplicantInrterpore Intl.
Decision Date1985-10-31
Product CodeDZC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPORE 200 POROUS HYDROXYAPATITE is the device name listed in this FDA 510(k) record. The listed applicant is Inrterpore Intl.. It received FDA 510(k) clearance on 1985-10-31 under 510(k) number K852975. The device is classified under product code DZC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERPORE 200 POROUS HYDROXYAPATITE?

INTERPORE 200 POROUS HYDROXYAPATITE is a medical device that received FDA 510(k) clearance on 1985-10-31. The listed applicant is Inrterpore Intl.. The 510(k) number is K852975.

When did INTERPORE 200 POROUS HYDROXYAPATITE receive FDA 510(k) clearance?

INTERPORE 200 POROUS HYDROXYAPATITE received FDA 510(k) clearance on 1985-10-31, under 510(k) number K852975.

Who is the listed applicant for INTERPORE 200 POROUS HYDROXYAPATITE?

The FDA 510(k) record lists Inrterpore Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERPORE 200 POROUS HYDROXYAPATITE?

The FDA product code for INTERPORE 200 POROUS HYDROXYAPATITE is DZC.

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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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