MC+

GUDID 03662663021739

MC+ OPEN V.B.R.14x15.5 H7MM

LDR Spine Usa, Inc.

Polymeric spinal fusion cage, sterile
Primary Device ID03662663021739
NIH Device Record Key4763a369-6d8f-409e-aafa-ca04aea01683
Commercial Distribution StatusIn Commercial Distribution
Brand NameMC+
Version Model NumberMC623P
Company DUNS615789729
Company NameLDR Spine Usa, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com
Phone512-344-3333
Emailsurgeoninfo@ldrspine.com

Device Dimensions

Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter
Width15.5 Millimeter
Depth14 Millimeter
Height7 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103662663021739 [Primary]

FDA Product Code

ODPIntervertebral Fusion Device With Bone Graft, Cervical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-18
Device Publish Date2015-10-24

On-Brand Devices [MC+]

03662663022132MC+ CLOSED V.B.R. 12x15.5H7MM
03662663022125MC+ CLOSED V.B.R. 12x15.5H6MM
03662663022118MC+ CLOSED V.B.R. 12x15. 5H5 MM
03662663022101MC+ CLOSED V.B.R. 12x15. 5H4,5 MM
03662663022064MC+ CLOSED V.B.R.12X14 H7 MM
03662663022057MC+ CLOSED V.B.R.12X14 H6 MM
03662663022040MC+ CLOSED V.B.R. 12X14 H5 MM
03662663022033MC+ CLOSED V.B.R. 12X14 H4.5 MM
03662663021999MC+ CLOSED V.B.R.14x17 H7 MM
03662663021982MC+ CLOSED V.B.R. 14x17 H6 MM
03662663021975MC+ CLOSED V.B.R. 14x17 H5 MM
03662663021937MC+ CLOSED V.B.R.14x15.5 H7 MM
03662663021920MC+ CLOSED V.B.R.14x15.5 H6 MM
03662663021913MC+ CLOSED V.B.R.14x15.5 H5 MM
03662663021906MC+ CLOSED V.B.R.14x15.5 H4.5 MM
03662663021869MC+ CLOSED V.B.R. 14x14 H7 MM
03662663021852MC+ CLOSED V.B.R.14x14 H6 MM
03662663021845MC+ CLOSED V.B.R.14x14 H5 MM
03662663021838MC+ CLOSED V.B.R.14X14 H4.5 MM
03662663021821MC+ OPEN V.B.R.12X15.5H7MM
03662663021814MC+ OPEN V.B.R.12X15.5H6MM
03662663021807MC+ OPEN V.B.R.12X15.5H5MM
03662663021760MC+ OPEN V.B.R.14x17 H7 MM
03662663021753MC+ OPEN V.B.R.14x17 H6 MM
03662663021746MC+ OPEN V.B.R.14x17 H5 MM
03662663021739MC+ OPEN V.B.R.14x15.5 H7MM
03662663021722MC+ OPEN V.B.R.14x15.5 H6 MM
03662663021708MC+ OPEN V.B.R.14X14 H7 MM
03662663021692MC+ OPEN V.B.R.14X14 H6 MM
03662663021685MC+ OPEN V.B.R.14X14 H5 MM
03662663044158MC936R
03662663043687MC909R
03662663043304MC901R
03662663046077MC990
03662663045506MC928R
03662663045490MC906R
03662663044332MC960R
03662663044325TRIAL CERVICAL IMPLANT 12X15.5 H10 MM
03662663044318TRIAL CERVICAL IMPLANT 12X15.5 H9 MM
03662663044301TRIAL CERVICAL IMPLANT 12X15.5 H8 MM
03662663044295TRIAL CERVICAL IMPLANT 12X14 H10 MM
03662663044288TRIAL CERVICAL IMPLANT 12X14 H9 MM
03662663044271TRIAL CERVICAL IMPLANT 12X14 H8 MM
03662663044264TRIAL CERVICAL IMPLANT 14X17 H10 MM
03662663044257TRIAL CERVICAL IMPLANT 14X17 H9 MM
03662663044240TRIAL CERVICAL IMPLANT 14X17 H8 MM
03662663044233TRIAL CERVICAL IMPLANT 14X15.5 H10 MM
03662663044226TRIAL CERVICAL IMPLANT 14X15.5 H9 MM
03662663044219TRIAL CERVICAL IMPLANT 14X15.5 H8 MM
03662663044202TRIAL CERVICAL IMPLANT 14X14 H10 MM

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