FDA UDI In Commercial Distribution 🇺🇸 United States

MASTERGRAFT® Contain

DI: 00643169585454 · Model: 7800555 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MASTERGRAFT® Contain
Primary DI
00643169585454
Version / Model
7800555
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-27
Public Version
4
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
c2e89b08-bd68-44f4-8797-c0479f9d5a26

Device Description

STRIP 7800555 MASTERGRAFT CONTAIN 5CM X2

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
MR Safe
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
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00643169585454

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151172 000

Device Sizes

Type Value Unit Text
Depth 1.2 Centimeter
Length 5.0 Centimeter
Height 2.0 Centimeter