FDA UDI In Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TL

DI: 00191375006367 · Model: 7107-0308 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TL
Primary DI
00191375006367
Version / Model
7107-0308
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
6
Public Version Date
2021-01-06
Public Version Status
Update
Public Device Record Key
ad1348be-1e6b-4b74-9dfc-0d59584a9a92

Device Description

Interbody Fusion Device 7 Degree 50 (M/L) 18 (A/P) 8 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
No
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00191375006367

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140055 000

Device Sizes

Type Value Unit Text
Angle 7 degree
Device Size Text, specify width(MLxAP), 50 x 18, mm
Height 8 Millimeter
Device Size Text, specify Lordotic Angle 7 Deg
Width 18 Millimeter
Length 50 Millimeter