FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology

DI: 00191375048060 · Model: 7120-0512-N · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TL Hyperlordotic nanoLOCK® Surface Technology
Primary DI
00191375048060
Version / Model
7120-0512-N
Catalog Number
7120-0512-N
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-15
Public Version
3
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
240ba61c-5318-4aea-bc9c-4f40740a0099
Distribution End Date
2020-09-18

Device Description

Interbody Fusion Device 20 Degree 60 (M/L) 18 (A/P) 12 mm

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 00191375048060

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Lordotic Angle - 20 Deg
Width 18 Millimeter
Angle 20 degree
Length 60 Millimeter
Height 12 Millimeter
Device Size Text, specify width(MLxAP), 60 x 18, mm