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FDA 510(k)

MICROFUSE PUTTY AND MICROFUSE ST MIS

K-Number: K102392 · 2010-12-22

ApplicantGlobus Medical, Inc.
Decision Date2010-12-22
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MICROFUSE PUTTY AND MICROFUSE ST MIS is the device name listed in this FDA 510(k) record. The listed applicant is Globus Medical, Inc.. It received FDA 510(k) clearance on 2010-12-22 under 510(k) number K102392. 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 MICROFUSE PUTTY AND MICROFUSE ST MIS?

MICROFUSE PUTTY AND MICROFUSE ST MIS is a medical device that received FDA 510(k) clearance on 2010-12-22. The listed applicant is Globus Medical, Inc.. The 510(k) number is K102392.

When did MICROFUSE PUTTY AND MICROFUSE ST MIS receive FDA 510(k) clearance?

MICROFUSE PUTTY AND MICROFUSE ST MIS received FDA 510(k) clearance on 2010-12-22, under 510(k) number K102392.

Who is the listed applicant for MICROFUSE PUTTY AND MICROFUSE ST MIS?

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

What is the FDA product code for MICROFUSE PUTTY AND MICROFUSE ST MIS?

The FDA product code for MICROFUSE PUTTY AND MICROFUSE ST MIS is MQV.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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