FDA 510(k)

POWEREASE SYSTEM

K-Number: K123270 · 2013-01-11

ApplicantMedtronic Sofamor Danek USA, Inc.

Decision Date2013-01-11

Product CodeHBE

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

POWEREASE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek USA, Inc.. It received FDA 510(k) clearance on 2013-01-11 under 510(k) number K123270. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWEREASE SYSTEM?

POWEREASE SYSTEM is a medical device that received FDA 510(k) clearance on 2013-01-11. The listed applicant is Medtronic Sofamor Danek USA, Inc.. The 510(k) number is K123270.

When did POWEREASE SYSTEM receive FDA 510(k) clearance?

POWEREASE SYSTEM received FDA 510(k) clearance on 2013-01-11, under 510(k) number K123270.

Who is the listed applicant for POWEREASE SYSTEM?

The FDA 510(k) record lists Medtronic Sofamor Danek USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWEREASE SYSTEM?

The FDA product code for POWEREASE SYSTEM is HBE.

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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.