FDA UDI In Commercial Distribution 🇺🇸 United States

SCARLET® AL-T Intervertebral body fusion device

DI: 07640178988071 · Model: SCA-LS 15 14-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
07640178988071
Version / Model
SCA-LS 15 14-S
Catalog Number
SCA-LS 15 14-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-07
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
73811899-fc0b-4376-8130-a9d34fdff44e

Device Description

Secured Lumbar Anterior Cage

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
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 07640178988071

Device Sizes

Type Value Unit Text
Height 14 Millimeter
Angle 15 degree