FDA UDI In Commercial Distribution 🇺🇸 United States

PROGENIX® PUTTY and PROGENIX® PLUS

DI: 00613994391018 · Model: 006001 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROGENIX® PUTTY and PROGENIX® PLUS
Primary DI
00613994391018
Version / Model
006001
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-20
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
093ca1b5-4321-4105-bec9-5d9923bd4ea9

Device Description

DBM 006001 PROGENIX PLUS 1CC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NUN BONE GRAFTING MATERIAL, HUMAN SOURCE

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Primary 00613994391018

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081950 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 cc volume

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
store at ambient temperature