Verteloc Lumbar Cage

GUDID 09348215129293

SIGNATURE ORTHOPAEDICS PTY LTD

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage
Primary Device ID09348215129293
NIH Device Record Key1cbb2196-bd36-4432-84bb-8fa868d68efc
Commercial Distribution StatusIn Commercial Distribution
Brand NameVerteloc Lumbar Cage
Version Model Number131-031-727
Company DUNS751993028
Company NameSIGNATURE ORTHOPAEDICS PTY LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS109348215129293 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-20
Device Publish Date2024-03-12

On-Brand Devices [Verteloc Lumbar Cage ]

09348215129682131-037-927
09348215129675131-037-923
09348215129668131-037-827
09348215129651131-037-823
09348215129644131-037-727
09348215129637131-037-723
09348215129620131-037-327
09348215129613131-037-323
09348215129606131-037-227
09348215129590131-037-223
09348215129583131-037-127
09348215129576131-037-123
09348215129552131-037-023
09348215129545131-039-527
09348215129408131-031-127
09348215129392131-031-527
09348215129385131-031-327
09348215129378131-031-227
09348215129361131-039-323
09348215129354131-039-223
09348215129347131-039-123
09348215129330131-039-023
09348215129323131-039-923
09348215129316131-031-027
09348215129309131-031-927
09348215129293131-031-727
09348215129286131-039-327
09348215129279131-039-227
09348215129262131-039-127
09348215129255131-039-027
09348215129248131-039-927
09348215129231131-037-527
09348215129224131-039-727

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.