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FDA 510(k)

NUVASIVE CEMENT RESTRICTOR

K-Number: K032180 · 2003-10-07

ApplicantNuvasive, Inc.
Decision Date2003-10-07
Product CodeJDK
Advisory CommitteeSU
DecisionUnknown

Device Summary

NUVASIVE CEMENT RESTRICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2003-10-07 under 510(k) number K032180. The device is classified under product code JDK. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NUVASIVE CEMENT RESTRICTOR?

NUVASIVE CEMENT RESTRICTOR is a medical device that received FDA 510(k) clearance on 2003-10-07. The listed applicant is Nuvasive, Inc.. The 510(k) number is K032180.

When did NUVASIVE CEMENT RESTRICTOR receive FDA 510(k) clearance?

NUVASIVE CEMENT RESTRICTOR received FDA 510(k) clearance on 2003-10-07, under 510(k) number K032180.

Who is the listed applicant for NUVASIVE CEMENT RESTRICTOR?

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 CEMENT RESTRICTOR?

The FDA product code for NUVASIVE CEMENT RESTRICTOR is JDK.

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Other records listing Nuvasive, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K240507NuVasive AttraX ScaffoldK223731NuVasive Modulus-C Interbody SystemK211757Simplify DiscK173117NuVasive® VersaTie™ SystemK133052AFFIX(R) NEXT GEN SPINOUS PROCESS PLATE SYSTEMK131025ARCHON ANTERIOR CERVICAL PLATE SYSTEM

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Related Devices (Code: JDK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K210062Mectaplug PE IIMedacta International S.A.K061465KMI CEMENT RESTRICTOR IMPLANTKinetikos Medical, Inc.K061698MODIFICATION TO LIFE SPINE CEMENT RESTRICTORLife SpineK060247LIFE SPINE CEMENT RESTRICTORLife SpineK060132SPINAL USA CEMENT RESTRICTOR SYSTEMSpinal USAK051371INTERBODY INNOVATIONS CEMENT RESTRICTORInterbody Innovations, Llp

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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