FDA UDI Not in Commercial Distribution 🇺🇸 United States

SCARLET® AL-T Intervertebral body fusion device

DI: 07640178986954 · Model: SJT-LS 55 60-S · SpineArt SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCARLET® AL-T Intervertebral body fusion device
Primary DI
07640178986954
Version / Model
SJT-LS 55 60-S
Catalog Number
SJT-LS 55 60-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-07
Public Version
7
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
854a1d10-c4db-492d-95fc-4dcaa289542f
Distribution End Date
2018-12-07

Device Description

Bone Screw

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
MR Conditional
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
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 07640178986954

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Length 60 Millimeter