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FDA 510(k)

INTERPORE CROSS CEMENT RESTRICTOR

K-Number: K023908 · 2003-05-16

ApplicantInterpore Cross Intl.
Decision Date2003-05-16
Product CodeJDK
Advisory CommitteeSU
DecisionUnknown

Device Summary

INTERPORE CROSS CEMENT RESTRICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Cross Intl.. It received FDA 510(k) clearance on 2003-05-16 under 510(k) number K023908. 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 INTERPORE CROSS CEMENT RESTRICTOR?

INTERPORE CROSS CEMENT RESTRICTOR is a medical device that received FDA 510(k) clearance on 2003-05-16. The listed applicant is Interpore Cross Intl.. The 510(k) number is K023908.

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

INTERPORE CROSS CEMENT RESTRICTOR received FDA 510(k) clearance on 2003-05-16, under 510(k) number K023908.

Who is the listed applicant for INTERPORE CROSS CEMENT RESTRICTOR?

The FDA 510(k) record lists Interpore Cross Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERPORE CROSS CEMENT RESTRICTOR?

The FDA product code for INTERPORE CROSS CEMENT RESTRICTOR is JDK.

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Other records listing Interpore Cross Intl. as applicant

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K050861PEEK CASK031399INTERGRO DBMK041407TITANIUM MESH IMPLANTK043229MODIFICATION TO ALTIUS OCT SYSTEMK042798C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEMK040928EXPANDABLE PEEK VBR IMPLANT

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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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