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FDA 510(k)

NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW

K-Number: K001323 · 2000-07-25

ApplicantNuvasive, Inc.
Decision Date2000-07-25
Product CodeMRW
DecisionSubstantially Equivalent

Device Summary

NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2000-07-25 under 510(k) number K001323. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW?

NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW is a medical device that received FDA 510(k) clearance on 2000-07-25. The listed applicant is Nuvasive, Inc.. The 510(k) number is K001323.

When did NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW receive FDA 510(k) clearance?

NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW received FDA 510(k) clearance on 2000-07-25, under 510(k) number K001323.

Who is the listed applicant for NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW?

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 PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW?

The FDA product code for NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW is MRW.

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Related Devices (Code: MRW)

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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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