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FDA 510(k)

CORIN BIOLOX DELTA FEMORAL HEADS

K-Number: K103120 · 2011-02-28

ApplicantCorin USA
Decision Date2011-02-28
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN BIOLOX DELTA FEMORAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2011-02-28 under 510(k) number K103120. 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 BIOLOX DELTA FEMORAL HEADS?

CORIN BIOLOX DELTA FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2011-02-28. The listed applicant is Corin USA. The 510(k) number is K103120.

When did CORIN BIOLOX DELTA FEMORAL HEADS receive FDA 510(k) clearance?

CORIN BIOLOX DELTA FEMORAL HEADS received FDA 510(k) clearance on 2011-02-28, under 510(k) number K103120.

Who is the listed applicant for CORIN BIOLOX DELTA FEMORAL HEADS?

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 BIOLOX DELTA FEMORAL HEADS?

The FDA product code for CORIN BIOLOX DELTA FEMORAL HEADS 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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