MASTERGRAFT® Contain

GUDID 00643169585478

STRIP 7800520 MASTERGRAFT CONTAIN 20CM

MEDTRONIC SOFAMOR DANEK, INC.

Bone matrix implant, synthetic
Primary Device ID00643169585478
NIH Device Record Key1cf0324d-2bcc-4789-a30f-28e7886815ea
Commercial Distribution StatusIn Commercial Distribution
Brand NameMASTERGRAFT® Contain
Version Model Number7800520
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Height2 Centimeter
Height2 Centimeter
Height2 Centimeter
Height2 Centimeter
Height2 Centimeter
Height2 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169585478 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQVFILLER, BONE VOID, CALCIUM COMPOUND

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-27

On-Brand Devices [MASTERGRAFT® Contain]

00643169585478STRIP 7800520 MASTERGRAFT CONTAIN 20CM
00643169585461STRIP 7800510 MASTERGRAFT CONTAIN 10CM
00643169585454STRIP 7800555 MASTERGRAFT CONTAIN 5CM X2
00643169585447STRIP 7800505 MASTERGRAFT CONTAIN 5CM

Trademark Results [MASTERGRAFT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MASTERGRAFT
MASTERGRAFT
78112930 2921419 Live/Registered
MEDTRONIC SOFAMOR DANEK USA, INC.
2002-03-06

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