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FDA 510(k)

ENDOBON XENOGRAFT GRANULES

K-Number: K110449 · 2011-05-13

ApplicantBiomet 3i
Decision Date2011-05-13
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOBON XENOGRAFT GRANULES is the device name listed in this FDA 510(k) record. The listed applicant is Biomet 3i. It received FDA 510(k) clearance on 2011-05-13 under 510(k) number K110449. 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 ENDOBON XENOGRAFT GRANULES?

ENDOBON XENOGRAFT GRANULES is a medical device that received FDA 510(k) clearance on 2011-05-13. The listed applicant is Biomet 3i. The 510(k) number is K110449.

When did ENDOBON XENOGRAFT GRANULES receive FDA 510(k) clearance?

ENDOBON XENOGRAFT GRANULES received FDA 510(k) clearance on 2011-05-13, under 510(k) number K110449.

Who is the listed applicant for ENDOBON XENOGRAFT GRANULES?

The FDA 510(k) record lists Biomet 3i as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOBON XENOGRAFT GRANULES?

The FDA product code for ENDOBON XENOGRAFT GRANULES is 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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