FDA UDI In Commercial Distribution 🇺🇸 United States

Triton

DI: 00840996184786 · Model: S-QT10-0845 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Triton
Primary DI
00840996184786
Version / Model
S-QT10-0845
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-03
Public Version
1
Public Version Date
2023-02-13
Public Version Status
New
Public Device Record Key
10923776-411a-4de5-a136-86c8c38cb8d1

Device Description

Triton,screws,S,8x45mm

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
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
OUR Sacroiliac joint fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00840996184786

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K211449 000