FDA UDI In Commercial Distribution 🇺🇸 United States

DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

DI: 00643169502390 · Model: 2150125 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
Primary DI
00643169502390
Version / Model
2150125
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-09
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b082d06c-3d60-4285-a7c9-d6c71f6048a9

Device Description

SCREW 2150125 SCREW 25MM

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
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
OVD Intervertebral fusion device with integrated fixation, lumbar
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00643169502390

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150135 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 25MM