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FDA 510(k)

CORIN MINIHIP FEMORAL STEM

K-Number: K111046 · 2011-06-29

ApplicantCorin USA
Decision Date2011-06-29
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN MINIHIP FEMORAL STEM is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2011-06-29 under 510(k) number K111046. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORIN MINIHIP FEMORAL STEM?

CORIN MINIHIP FEMORAL STEM is a medical device that received FDA 510(k) clearance on 2011-06-29. The listed applicant is Corin USA. The 510(k) number is K111046.

When did CORIN MINIHIP FEMORAL STEM receive FDA 510(k) clearance?

CORIN MINIHIP FEMORAL STEM received FDA 510(k) clearance on 2011-06-29, under 510(k) number K111046.

Who is the listed applicant for CORIN MINIHIP FEMORAL STEM?

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

What is the FDA product code for CORIN MINIHIP FEMORAL STEM?

The FDA product code for CORIN MINIHIP FEMORAL STEM is LZO.

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Other records listing Corin USA as applicant

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Related Devices (Code: LZO)

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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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