FDA UDI In Commercial Distribution 🇺🇸 United States

CAPSTONE® Spinal System

DI: 00643169410480 · Model: X0613893 · 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
00643169410480
Version / Model
X0613893
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ad4c9063-b317-4230-84a7-4b5dccc2ea7a

Device Description

SPACER X0613893 STERILE 3DEG 8X12X26

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 00643169410480

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133650 000

Device Sizes

Type Value Unit Text
Angle 3.0 degree
Height 12.0 Millimeter
Width 8.0 Millimeter
Length 26.0 Millimeter