FDA UDI In Commercial Distribution 🇺🇸 United States

BALLOON KYPHOPLASTY ESSENTIALS

DI: 00763000031879 · Model: NH152PB · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BALLOON KYPHOPLASTY ESSENTIALS
Primary DI
00763000031879
Version / Model
NH152PB
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-26
Public Version
1
Public Version Date
2019-02-26
Public Version Status
New
Public Device Record Key
b010eacd-b6d2-4aed-a518-00bed71c1bc5

Device Description

KIT NH152PB 15/2 SPINE ESSEN FF

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
HRX Arthroscope

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Primary 00763000031879

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K041454 000
K151532 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place