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FDA 510(k)

MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM

K-Number: K070273 · 2007-04-03

ApplicantNuvasive, Inc.
Decision Date2007-04-03
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO NUVASIVE LATERAL 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 2007-04-03 under 510(k) number K070273. 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 MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM?

MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2007-04-03. The listed applicant is Nuvasive, Inc.. The 510(k) number is K070273.

When did MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM received FDA 510(k) clearance on 2007-04-03, under 510(k) number K070273.

Who is the listed applicant for MODIFICATION TO NUVASIVE LATERAL 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 MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM?

The FDA product code for MODIFICATION TO NUVASIVE LATERAL 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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