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FDA 510(k)

LIGATURE CARRIER/PACKER, HYDROXYLAPATITE

K-Number: K874342 · 1987-11-13

ApplicantCox-Uphuff Intl.
Decision Date1987-11-13
Product CodeGEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGATURE CARRIER/PACKER, HYDROXYLAPATITE is the device name listed in this FDA 510(k) record. The listed applicant is Cox-Uphuff Intl.. It received FDA 510(k) clearance on 1987-11-13 under 510(k) number K874342. The device is classified under product code GEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGATURE CARRIER/PACKER, HYDROXYLAPATITE?

LIGATURE CARRIER/PACKER, HYDROXYLAPATITE is a medical device that received FDA 510(k) clearance on 1987-11-13. The listed applicant is Cox-Uphuff Intl.. The 510(k) number is K874342.

When did LIGATURE CARRIER/PACKER, HYDROXYLAPATITE receive FDA 510(k) clearance?

LIGATURE CARRIER/PACKER, HYDROXYLAPATITE received FDA 510(k) clearance on 1987-11-13, under 510(k) number K874342.

Who is the listed applicant for LIGATURE CARRIER/PACKER, HYDROXYLAPATITE?

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

What is the FDA product code for LIGATURE CARRIER/PACKER, HYDROXYLAPATITE?

The FDA product code for LIGATURE CARRIER/PACKER, HYDROXYLAPATITE is GEJ.

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Other records listing Cox-Uphuff Intl. as applicant

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Related Devices (Code: GEJ)

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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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