FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TAS Sterile Barrier System

DI: 00191375038931 · Model: 2303-1417-S · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TAS Sterile Barrier System
Primary DI
00191375038931
Version / Model
2303-1417-S
Catalog Number
2303-1417-S
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-30
Public Version
4
Public Version Date
2023-06-27
Public Version Status
Update
Public Device Record Key
368a79ed-484d-4ca4-b718-c23f151c36d3
Distribution End Date
2020-03-12

Device Description

Plate , X-Large, 14mm to 17mm

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
Yes
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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00191375038931

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Footprint, X-Large
Device Size Text, specify For Use with Heights, 14mm to 17mm
Height 15 Millimeter
Height 14 Millimeter
Height 17 Millimeter
Height 16 Millimeter