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FDA 510(k)

MINIHIP STEM

K-Number: K083312 · 2010-04-05

ApplicantCorin USA
Decision Date2010-04-05
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

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 2010-04-05 under 510(k) number K083312. 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 MINIHIP STEM?

MINIHIP STEM is a medical device that received FDA 510(k) clearance on 2010-04-05. The listed applicant is Corin USA. The 510(k) number is K083312.

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

MINIHIP STEM received FDA 510(k) clearance on 2010-04-05, under 510(k) number K083312.

Who is the listed applicant for 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 MINIHIP STEM?

The FDA product code for MINIHIP STEM is LZO.

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Related Devices (Code: LZO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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