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FDA 510(k)

VARIOUS

K-Number: K112417 · 2012-01-13

ApplicantDepuy Mitek, A Johnson & Johnson Company
Decision Date2012-01-13
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Mitek, A Johnson & Johnson Company. It received FDA 510(k) clearance on 2012-01-13 under 510(k) number K112417. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIOUS?

VARIOUS is a medical device that received FDA 510(k) clearance on 2012-01-13. The listed applicant is Depuy Mitek, A Johnson & Johnson Company. The 510(k) number is K112417.

When did VARIOUS receive FDA 510(k) clearance?

VARIOUS received FDA 510(k) clearance on 2012-01-13, under 510(k) number K112417.

Who is the listed applicant for VARIOUS?

The FDA 510(k) record lists Depuy Mitek, A Johnson & Johnson Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIOUS?

The FDA product code for VARIOUS is MBI.

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Other records listing Depuy Mitek, A Johnson & Johnson Company as applicant

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Related Devices (Code: MBI)

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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