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FDA 510(k)

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM

K-Number: K090176 · 2009-04-27

ApplicantNuvasive, Inc.
Decision Date2009-04-27
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2009-04-27 under 510(k) number K090176. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM?

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2009-04-27. The listed applicant is Nuvasive, Inc.. The 510(k) number is K090176.

When did NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM receive FDA 510(k) clearance?

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM received FDA 510(k) clearance on 2009-04-27, under 510(k) number K090176.

Who is the listed applicant for NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM?

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

What is the FDA product code for NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM?

The FDA product code for NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM is MQP.

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Other records listing Nuvasive, Inc. as applicant

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Related Devices (Code: MQP)

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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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