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FDA 510(k)

NUVASIVE TRAVERSE PLATE SYSTEM

K-Number: K103750 · 2011-03-03

ApplicantNuvasive, Inc.
Decision Date2011-03-03
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NUVASIVE TRAVERSE PLATE 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 2011-03-03 under 510(k) number K103750. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE TRAVERSE PLATE SYSTEM?

NUVASIVE TRAVERSE PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2011-03-03. The listed applicant is Nuvasive, Inc.. The 510(k) number is K103750.

When did NUVASIVE TRAVERSE PLATE SYSTEM receive FDA 510(k) clearance?

NUVASIVE TRAVERSE PLATE SYSTEM received FDA 510(k) clearance on 2011-03-03, under 510(k) number K103750.

Who is the listed applicant for NUVASIVE TRAVERSE PLATE 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 TRAVERSE PLATE SYSTEM?

The FDA product code for NUVASIVE TRAVERSE PLATE SYSTEM is KWQ.

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Other records listing Nuvasive, Inc. as applicant

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Related Devices (Code: KWQ)

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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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