FDA UDI In Commercial Distribution 🇺🇸 United States

CAPSTONE® Spinal System

DI: 00643169410152 · Model: X0613920 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CAPSTONE® Spinal System
Primary DI
00643169410152
Version / Model
X0613920
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
bda888dd-5ffc-469a-888d-444a22ae09a2

Device Description

SPACER X0613920 STERILE 3DEG 10X11X22

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

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

Identifiers

Type ID
Primary 00643169410152

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133650 000

Device Sizes

Type Value Unit Text
Length 22.0 Millimeter
Height 11.0 Millimeter
Angle 3.0 degree
Width 10.0 Millimeter