FDA UDI In Commercial Distribution 🇺🇸 United States

THUNDERBOLT

DI: 00840996189644 · Model: MT11-4590-120 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
THUNDERBOLT
Primary DI
00840996189644
Version / Model
MT11-4590-120
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-06
Public Version
1
Public Version Date
2023-07-14
Public Version Status
New
Public Device Record Key
40241d4d-ad65-4829-9d81-cb07a96215e6

Device Description

THUNDERBOLT,X-TAB SCREW,4.5X90X120

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00840996189644

Premarket Submissions

Submission Number Supplement Number
K171456 000