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FDA 510(k)

NBD CEMENT RESTRICTOR DEVICE

K-Number: K021788 · 2002-10-04

ApplicantNew Business Development, LLC
Decision Date2002-10-04
Product CodeJDK
Advisory CommitteeSU
DecisionUnknown

Device Summary

NBD CEMENT RESTRICTOR DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is New Business Development, LLC. It received FDA 510(k) clearance on 2002-10-04 under 510(k) number K021788. 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 NBD CEMENT RESTRICTOR DEVICE?

NBD CEMENT RESTRICTOR DEVICE is a medical device that received FDA 510(k) clearance on 2002-10-04. The listed applicant is New Business Development, LLC. The 510(k) number is K021788.

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

NBD CEMENT RESTRICTOR DEVICE received FDA 510(k) clearance on 2002-10-04, under 510(k) number K021788.

Who is the listed applicant for NBD CEMENT RESTRICTOR DEVICE?

The FDA 510(k) record lists New Business Development, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NBD CEMENT RESTRICTOR DEVICE?

The FDA product code for NBD CEMENT RESTRICTOR DEVICE is JDK.

Related Clinical Trials

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.

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Other records listing New Business Development, LLC 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.

K072029PHENIX VERTEBRAL BODY REPLACEMENTK050377NBD HEAD SCREWK032196NBD DISPOSABLE RF CANNULAE

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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