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FDA 510(k)

MIIG SR

K-Number: K060011 · 2006-02-27

ApplicantWrightmedicaltechnologyinc
Decision Date2006-02-27
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MIIG SR is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2006-02-27 under 510(k) number K060011. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIIG SR?

MIIG SR is a medical device that received FDA 510(k) clearance on 2006-02-27. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K060011.

When did MIIG SR receive FDA 510(k) clearance?

MIIG SR received FDA 510(k) clearance on 2006-02-27, under 510(k) number K060011.

Who is the listed applicant for MIIG SR?

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

What is the FDA product code for MIIG SR?

The FDA product code for MIIG SR is MQV.

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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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