STALIF MIDLINE

GUDID 00815101029306

Centinel Spine, Inc.

Metal-polymer composite spinal interbody fusion cage
Primary Device ID00815101029306
NIH Device Record Key47b293a0-3a82-4669-92ec-7e6730fa50e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTALIF MIDLINE
Version Model NumberSTM6030
Company DUNS949024850
Company NameCentinel Spine, Inc.
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 Datefalse
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
GS100815101029306 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-02-24
Device Publish Date2017-03-20

On-Brand Devices [STALIF MIDLINE]

00815101029344STM6035R
00815101029337STM6030R
00815101029320STM6025R
00815101029313STM6035
00815101029306STM6030
00815101029290STM6025

Trademark Results [STALIF MIDLINE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
STALIF MIDLINE
STALIF MIDLINE
77874913 4003160 Live/Registered
CENTINEL SPINE, LLC
2009-11-17

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