FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TA VBR

DI: 00191375035992 · Model: 2156-9318 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TA VBR
Primary DI
00191375035992
Version / Model
2156-9318
Catalog Number
2156-9318
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
2020-12-09
Public Version Status
Update
Public Device Record Key
1d3c7882-513f-4a24-bc1f-fa0338352ec4
Distribution End Date
2020-09-18

Device Description

Trial, 7 Deg Lordotic, X-Large, 18mm

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
MQP Spinal vertebral body replacement device

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00191375035992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K032812 000

Device Sizes

Type Value Unit Text
Angle 7 degree
Depth 27 Millimeter
Device Size Text, specify width(MLxAP), 40 x 27, mm
Device Size Text, specify Lordotic Angle 7 Deg
Height 18 Millimeter
Width 40 Millimeter