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FDA 510(k)

TRANSITION STABILIZATION SYSTEM

K-Number: K073439 · 2009-02-20

ApplicantGlobus Medical, Inc.
Decision Date2009-02-20
Product CodeNQP
Advisory CommitteeOR
DecisionUnknown

Device Summary

TRANSITION STABILIZATION SYSTEM 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 2009-02-20 under 510(k) number K073439. The device is classified under product code NQP. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TRANSITION STABILIZATION SYSTEM?

TRANSITION STABILIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 2009-02-20. The listed applicant is Globus Medical, Inc.. The 510(k) number is K073439.

When did TRANSITION STABILIZATION SYSTEM receive FDA 510(k) clearance?

TRANSITION STABILIZATION SYSTEM received FDA 510(k) clearance on 2009-02-20, under 510(k) number K073439.

Who is the listed applicant for TRANSITION STABILIZATION SYSTEM?

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 TRANSITION STABILIZATION SYSTEM?

The FDA product code for TRANSITION STABILIZATION SYSTEM is NQP.

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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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