FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON TL

DI: M682720072130 · Model: 7200-7213 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON TL
Primary DI
M682720072130
Version / Model
7200-7213
Catalog Number
7200-7213
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
6
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
72e827aa-30e6-43f8-906b-e9346f396213
Distribution End Date
2020-09-21

Device Description

PARALLEL, RASP, 22X13MM

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
Yes
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary M682720072130

Customer Contacts

Device Sizes

Type Value Unit Text
Width 22 Millimeter
Height 13 Millimeter
Device Size Text, specify Height 13mm, Width 22mm, Lordotic Angle 7 Deg
Angle 7 degree