FDA UDI In Commercial Distribution 🇺🇸 United States

CAPSTONE® Spinal System

DI: 00613994290946 · Model: 2991232 · 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
00613994290946
Version / Model
2991232
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-20
Public Version
3
Public Version Date
2023-10-20
Public Version Status
Update
Public Device Record Key
05786eed-e365-4a09-b913-6b9dc38b0c57

Device Description

SPACER 2991232 CAPSTONE PEEK 12X32

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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00613994290946

Customer Contacts

Device Sizes

Type Value Unit Text
Length 32.0 Millimeter
Outer Diameter 12.0 Millimeter