CervAlign™ Anterior Cervical Plate System

Appliance, Fixation, Spinal Intervertebral Body

Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.)

The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. (dba Rti Surgical, Inc.) with the FDA for Cervalign™ Anterior Cervical Plate System.

Pre-market Notification Details

Device IDK183060
510k NumberK183060
Device Name:CervAlign™ Anterior Cervical Plate System
ClassificationAppliance, Fixation, Spinal Intervertebral Body
Applicant Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) 375 River Park Circle Marquette,  MI  49855
ContactJaclyn Holli
CorrespondentJaclyn Holli
Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) 375 River Park Circle Marquette,  MI  49855
Product CodeKWQ  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-11-02
Decision Date2019-01-17
Summary:summary

NIH GUDID Devices

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Trademark Results [CervAlign]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CERVALIGN
CERVALIGN
88037029 not registered Live/Pending
Pioneer Surgical Technology, Inc.
2018-07-13

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