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FDA 510(k)

CORIN MINIHIP STEM

K-Number: K131986 · 2013-12-16

ApplicantCorin USA
Decision Date2013-12-16
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN MINIHIP 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 2013-12-16 under 510(k) number K131986. 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 STEM?

CORIN MINIHIP STEM is a medical device that received FDA 510(k) clearance on 2013-12-16. The listed applicant is Corin USA. The 510(k) number is K131986.

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

CORIN MINIHIP STEM received FDA 510(k) clearance on 2013-12-16, under 510(k) number K131986.

Who is the listed applicant for CORIN MINIHIP 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 STEM?

The FDA product code for CORIN MINIHIP STEM is 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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