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FDA 510(k)

CORIN ADAPTOR SLEEVE

K-Number: K071471 · 2007-09-10

ApplicantHowmedica Osteonics Corp.
Decision Date2007-09-10
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN ADAPTOR SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2007-09-10 under 510(k) number K071471. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORIN ADAPTOR SLEEVE?

CORIN ADAPTOR SLEEVE is a medical device that received FDA 510(k) clearance on 2007-09-10. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K071471.

When did CORIN ADAPTOR SLEEVE receive FDA 510(k) clearance?

CORIN ADAPTOR SLEEVE received FDA 510(k) clearance on 2007-09-10, under 510(k) number K071471.

Who is the listed applicant for CORIN ADAPTOR SLEEVE?

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

What is the FDA product code for CORIN ADAPTOR SLEEVE?

The FDA product code for CORIN ADAPTOR SLEEVE is KWL.

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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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