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FDA 510(k)

INTERBODY INNOVATIONS CEMENT RESTRICTOR

K-Number: K051371 · 2005-12-06

ApplicantInterbody Innovations, Llp
Decision Date2005-12-06
Product CodeJDK
Advisory CommitteeSU
DecisionUnknown

Device Summary

INTERBODY INNOVATIONS CEMENT RESTRICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Interbody Innovations, Llp. It received FDA 510(k) clearance on 2005-12-06 under 510(k) number K051371. 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 INTERBODY INNOVATIONS CEMENT RESTRICTOR?

INTERBODY INNOVATIONS CEMENT RESTRICTOR is a medical device that received FDA 510(k) clearance on 2005-12-06. The listed applicant is Interbody Innovations, Llp. The 510(k) number is K051371.

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

INTERBODY INNOVATIONS CEMENT RESTRICTOR received FDA 510(k) clearance on 2005-12-06, under 510(k) number K051371.

Who is the listed applicant for INTERBODY INNOVATIONS CEMENT RESTRICTOR?

The FDA 510(k) record lists Interbody Innovations, Llp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERBODY INNOVATIONS CEMENT RESTRICTOR?

The FDA product code for INTERBODY INNOVATIONS CEMENT RESTRICTOR is JDK.

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Other records listing Interbody Innovations, Llp 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.

K081614ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGESK073105PEEK SPINAL SPHERESK062992SPINAL SPHERES

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 USAK051836SKELITE RESORBABLE CEMENT RESTRICTORMillenium Biologix, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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