FDA UDI In Commercial Distribution 🇺🇸 United States

THUNDERBOLT™ Minimally Invasive Pedicle Screw Systems

DI: 00840996114233 · Model: MT50-85100 · Choice Spine, LP
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
THUNDERBOLT™ Minimally Invasive Pedicle Screw Systems
Primary DI
00840996114233
Version / Model
MT50-85100
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
5
Public Version Date
2022-09-29
Public Version Status
Update
Public Device Record Key
d7c5fa16-5236-40e3-8b49-7848164421dc

Device Description

TBOLT,RED. SCREW ASSY,CANNULATED,8.5X100

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
MNH Orthosis, spondylolisthesis spinal fixation
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

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

Identifiers

Type ID
Primary 00840996114233

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132049 000

Device Sizes

Type Value Unit Text
Outer Diameter 8.5 Millimeter
Length 100 Millimeter