FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON TAS

DI: M682211292170 · Model: 2112-9217 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON TAS
Primary DI
M682211292170
Version / Model
2112-9217
Catalog Number
2112-9217
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
5
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
fe343fce-0bc9-4ea5-a467-aa4319be38e4
Distribution End Date
2020-09-21

Device Description

12 DEG LORDOTIC, TRIAL, LARGE, 17MM

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary M682211292170

Customer Contacts

Device Sizes

Type Value Unit Text
Height 17 Millimeter
Device Size Text, specify Lordotic Angle 12 Deg
Device Size Text, specify width(MLxAP), 36 x 24, mm
Angle 12 degree
Depth 24 Millimeter
Width 36 Millimeter