FDA UDI In Commercial Distribution 🇺🇸 United States

KyphPak® First Fracture Tray

DI: 00643169671683 · Model: KPX103RB-CDS · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KyphPak® First Fracture Tray
Primary DI
00643169671683
Version / Model
KPX103RB-CDS
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-03
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
42fa550b-c3bc-4b6c-b55d-18a3f92ac01e

Device Description

KIT KPX103RB-CDS 10/3 FF OSTEO WITH CDS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
HXG TAMP
HRX ARTHROSCOPE

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Primary 00643169671683

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103231 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool dry place (at max 25°C/77°F)