THUNDERBOLT Minimally Invasive Pedicle Screw System

GUDID 00840996187862

TBOLT,UNIVERSAL SCREWDRIVER, NEW THREAD

Choice Spine, LP

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00840996187862
NIH Device Record Keyd071a4e6-c3e2-44a4-8078-adf2b1d3bd21
Commercial Distribution StatusIn Commercial Distribution
Brand NameTHUNDERBOLT Minimally Invasive Pedicle Screw System
Version Model NumberM070-0160
Company DUNS078293017
Company NameChoice Spine, LP
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 Usefalse
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
GS100840996187862 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


[00840996187862]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-14
Device Publish Date2023-07-06

On-Brand Devices [THUNDERBOLT Minimally Invasive Pedicle Screw System]

00840996175050THUNDERBOLT,ROD CALIPER,SIDE MARKED
00840996175043THUNDERBOLT,REDUCER,LARGE T
00840996175036THUNDERBOLT,EXTERNAL REDUCER
00840996171250THUNDERBOLT,UNIVERSAL SCREWDRIVER
00840996170703THUNDERBOLT,TAP,7.5,40DEG TIP
00840996170697THUNDERBOLT,TAP,6.5,40DEG TIP
00840996170680THUNDERBOLT,TAP,5.5,40DEG TIP
00840996192859THUNDERBOLT,7.0 TAP FOR 7.5 SCREW
00840996192842THUNDERBOLT,6.0 TAP FOR 6.5 SCREW
00840996192835THUNDERBOLT,5.0 TAP FOR 5.5 SCREW
00840996192828THUNDERBOLT,4.0 TAP FOR 4.5 SCREW
00840996188258THUNDERBOLT,1/4 SQUARE SET SCREW DRIVER
00840996187862TBOLT,UNIVERSAL SCREWDRIVER, NEW THREAD

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