FDA UDI In Commercial Distribution 🇺🇸 United States

KyphoPak™ Tray

DI: 00643169102941 · Model: KPT1505 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KyphoPak™ Tray
Primary DI
00643169102941
Version / Model
KPT1505
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-16
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
fd43fbff-ecbc-487f-a56d-e8089e6f84c4

Device Description

KIT KPT1505 KYPAK TRY 15/3 FF W/ONESTEP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
HRX ARTHROSCOPE

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Primary 00643169102941

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K041454 000