FDA 510(k)

CAVUX Cervical Cage

K-Number: K161642 · 2016-10-07

ApplicantProvidence Medical Technology, Inc.

Decision Date2016-10-07

Product CodeODP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CAVUX Cervical Cage is a medical device manufactured by Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2016-10-07 under approval number K161642. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAVUX Cervical Cage?

CAVUX Cervical Cage is a medical device that received FDA 510(k) clearance on 2016-10-07. It is manufactured by Providence Medical Technology, Inc.. The 510(k) number is K161642.

When was CAVUX Cervical Cage approved by the FDA?

CAVUX Cervical Cage received FDA 510(k) clearance on 2016-10-07, under approval number K161642.

What company makes CAVUX Cervical Cage?

CAVUX Cervical Cage is manufactured by Providence Medical Technology, Inc..

What is the FDA product code for CAVUX Cervical Cage?

The FDA product code for CAVUX Cervical Cage is ODP.

Other Devices by Providence Medical Technology, Inc.

K172279PMT Posterior Fixation System K170698ALLY(TM) Bone Screws K163474CAVUX CervicalCage-L SA System K163374ALLY Facet Screws K180876DTRAX Spinal System K183589PMT Facet Screw

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Related Devices (Code: ODP)

K161127The Small PLATEAU (PLATEAU-C) Spacer SystemLife Spine, Inc. K162003IMSE Cervical CageThe Institute of Musculoskeletal Science & Education K160222OIC Cervical PEEK SpacerThe Orthopaedic Implant Company K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageDio Medical Co., Ltd. K161649Virtu C Spinal Implant SystemMet 1 Technologies, LLC

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.