FDA UDI In Commercial Distribution 🇺🇸 United States

Tiger Shark System

DI: 00840996166553 · Model: S-VT12-50221215 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tiger Shark System
Primary DI
00840996166553
Version / Model
S-VT12-50221215
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
10b3f78e-bb07-4933-89f7-c9456e7d3649

Device Description

TIGER SHARK,STERILE,LAT,50X22X15,12DEG

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
43084 Intervertebral-body internal spinal fixation system

Identifiers

Type ID
Primary 00840996166553

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K172816 000

Device Sizes

Type Value Unit Text
Height 15 Millimeter
Width 22 Millimeter
Length 50 Millimeter