WAVE O CAGE

Intervertebral Fusion Device With Bone Graft, Lumbar

ADVANCED MEDICAL TECHNOLOGIES AG

The following data is part of a premarket notification filed by Advanced Medical Technologies Ag with the FDA for Wave O Cage.

Pre-market Notification Details

Device IDK121330
510k NumberK121330
Device Name:WAVE O CAGE
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant ADVANCED MEDICAL TECHNOLOGIES AG 1001 OAKWOOD BLVD. Round Rock,  TX  78681
ContactJ.d. Webb
CorrespondentJ.d. Webb
ADVANCED MEDICAL TECHNOLOGIES AG 1001 OAKWOOD BLVD. Round Rock,  TX  78681
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2012-05-03
Decision Date2012-06-29
Summary:summary

NIH GUDID Devices

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