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FDA 510(k)

NUVASIVE LONG LATERAL SPINAL SYSTEM

K-Number: K111410 · 2011-06-20

ApplicantNuvasive, Inc.
Decision Date2011-06-20
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NUVASIVE LONG LATERAL SPINAL 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 2011-06-20 under 510(k) number K111410. 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 LONG LATERAL SPINAL SYSTEM?

NUVASIVE LONG LATERAL SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2011-06-20. The listed applicant is Nuvasive, Inc.. The 510(k) number is K111410.

When did NUVASIVE LONG LATERAL SPINAL SYSTEM receive FDA 510(k) clearance?

NUVASIVE LONG LATERAL SPINAL SYSTEM received FDA 510(k) clearance on 2011-06-20, under 510(k) number K111410.

Who is the listed applicant for NUVASIVE LONG LATERAL SPINAL 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 LONG LATERAL SPINAL SYSTEM?

The FDA product code for NUVASIVE LONG LATERAL SPINAL SYSTEM is 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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