PLEXUR P®

GUDID 00643169218062

SHEET 60000525 PLEXUR P 100MMX25MMX4MM

MEDTRONIC SOFAMOR DANEK, INC.

Cadaveric-donor/synthetic polymer bone graft
Primary Device ID00643169218062
NIH Device Record Key64596ca0-29fc-4e60-99b5-81f5a074f79a
Commercial Distribution Discontinuation2017-02-09
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePLEXUR P®
Version Model Number60000525
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Producttrue
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numbertrue
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

Width25 Millimeter
Width25 Millimeter
Width25 Millimeter
Width25 Millimeter
Width25 Millimeter
Width25 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169218062 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MBPFiller, bone void, osteoinduction (w/o human growth factor)

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 Date2015-07-20

On-Brand Devices [PLEXUR P®]

00613994986672GRANULES 6000-010 PLEXUR P 10CC
00613994986665GRANULES 6000-020 PLEXUR P 20CC
00613994986658GRANULES 6000-030 PLEXUR P 30CC
00613994986641CYLINDER 6000-107 PLEXUR P 7MMX25MM
00613994986634CYLINDER 6000-109 PLEXUR P 9MMX25MM
00613994986627CYLINDER 6000-111 PLEXUR P 11MMX25MM
00613994986610WEDGE 6000-210 PLEXUR P 40MMX15MMX10 DEG
00613994986603WEDGE 6000-215 PLEXUR P 40MMX15MMX15 DEG
00613994986597BLOCK 6000-310 PLEXUR P 10MMX10MMX20MM
00613994986580BLOCK 6000-320 PLEXUR P 20MMX20MMX20MM
00613994986573SHEET 6000-425 PLEXUR P 50MMX25MMX4MM
00613994986566SHEET 6000-525 PLEXUR P 100MMX25MMX4MM
00643169218307GRANULES 60000005 PLEXUR P 5CC
00643169218284GRANULES 60000010 PLEXUR P 10CC
00643169218277GRANULES 60000010INT PLEXUR P 10CC
00643169218260GRANULES 60000020 PLEXUR P 20 CC
00643169218253GRANULES 60000020INT PLEXUR P 20 CC
00643169218246GRANULES 60000030 PLEXUR P 30 CC
00643169218239GRANULES 60000030INT PLEXUR P 30 CC
00643169218222CYLINDER 60000107 PLEXUR P 7MMX25MM
00643169218208CYLINDER 60000109 PLEXUR P 9MMX25MM
00643169218185CYLINDER 60000111 PLEXUR P 11MMX25MM
00643169218161WEDGE 60000210 PLEXUR P 40MMX15MMX10
00643169218147WEDGE 60000215 PLEXUR P 40MMX15MMX15
00643169218130WEDGE 60000215INT PLEXUR P 40MMX15MMX15
00643169218123BLOCK 60000310 PLEXUR P 10MMX10MMX20MM
00643169218116BLCK 60000310INT PLEXUR P 10MMX10MMX20MM
00643169218109BLOCK 60000320 PLEXUR P 20MMX20MMX20MM
00643169218093BLCK 60000320INT PLEXUR P 20MMX20MMX20MM
00643169218086SHEET 60000425 PLEXUR P 50MMX25MMX4MM
00643169218062SHEET 60000525 PLEXUR P 100MMX25MMX4MM

Trademark Results [PLEXUR P]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PLEXUR P
PLEXUR P
77294070 3444563 Dead/Cancelled
Osteotech, Inc.
2007-10-02
PLEXUR P
PLEXUR P
77294057 3444561 Dead/Cancelled
Osteotech, Inc.
2007-10-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.