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FDA 510(k)

POROUS HYDROXYAPATITE BG200

K-Number: K841201 · 1984-08-03

ApplicantInterpore Intl.
Decision Date1984-08-03
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POROUS HYDROXYAPATITE BG200 is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1984-08-03 under 510(k) number K841201. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POROUS HYDROXYAPATITE BG200?

POROUS HYDROXYAPATITE BG200 is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Interpore Intl.. The 510(k) number is K841201.

When did POROUS HYDROXYAPATITE BG200 receive FDA 510(k) clearance?

POROUS HYDROXYAPATITE BG200 received FDA 510(k) clearance on 1984-08-03, under 510(k) number K841201.

Who is the listed applicant for POROUS HYDROXYAPATITE BG200?

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 POROUS HYDROXYAPATITE BG200?

The FDA product code for POROUS HYDROXYAPATITE BG200 is LYC.

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Related Devices (Code: LYC)

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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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