Centerline Cannulated Accessories

GUDID 00190837021153

Life Spine, Inc.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00190837021153
NIH Device Record Key05c81a72-286d-4800-a755-254742e6ec36
Commercial Distribution StatusIn Commercial Distribution
Brand NameCenterline Cannulated Accessories
Version Model Number6875-075
Company DUNS183641617
Company NameLife 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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100190837021153 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NKBThoracolumbosacral Pedicle Screw System

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


[00190837021153]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-12-12

On-Brand Devices [Centerline Cannulated Accessories]

001908370212146875-115
001908370212076875-105
001908370211916875-095
001908370211846875-090
001908370211776875-085
001908370211606875-080
001908370211536875-075
001908370211466875-070
001908370211396875-065
001908370211226875-060
001908370211156875-055
001908370211086875-050
001908370210926875-045
001908370210856875-040
001908370210786875-035
001908370210616875-030
001908370210544065-45-40
001908370210474065-40-40
001908370210304055-45-40
001908370210234055-40-40

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