InterBRIDGE

GUDID 03662663017503

H12mm Insert

LDR Spine Usa, Inc.

Lumbar interspinous decompression spacer, sterile
Primary Device ID03662663017503
NIH Device Record Key4959b545-cb4a-4d51-8f0a-e060139973a6
Commercial Distribution StatusIn Commercial Distribution
Brand NameInterBRIDGE
Version Model NumberIB0012T
Company DUNS615789729
Company NameLDR Spine Usa, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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
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

Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter
Height12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103662663017503 [Primary]

FDA Product Code

PEKSpinous Process Plate

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-03-10
Device Publish Date2015-10-24

On-Brand Devices [InterBRIDGE]

03662663037495IB9023R
03662663037488IB9022R
03662663037471IB9021R
03662663026253LOCKING ROD
03662663026246IMPLANT HOLDER
03662663026307IB990
03662663037457TRIAL H16MM
03662663037440TRIAL H14MM
03662663037433TRIAL H12MM
03662663037426TRIAL H10MM
03662663037419TRIAL H08MM
03662663037402IB9003R
03662663026291ASSEMBLY CLIP M
03662663026284ASSEMBLY CLIP S
03662663026277IB9031R
03662663026260IMPLANT HOLDER HANDLE
03662663024372IB9027R
03662663017541Locking plate M
03662663017534Locking plate S
03662663017527H16mm Insert
03662663017510H14mm Insert
03662663017503H12mm Insert
03662663017497H10mm Insert
03662663017480H08mm Insert
03662663004671H6.5mm Insert
03662663003087TRIAL H06.5MM

Trademark Results [InterBRIDGE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
INTERBRIDGE
INTERBRIDGE
97389506 not registered Live/Pending
Albert Moellenbeck
2022-04-29
INTERBRIDGE
INTERBRIDGE
85811003 4813235 Live/Registered
LDR Medical, S.A.S.
2012-12-27
INTERBRIDGE
INTERBRIDGE
73604760 1462551 Dead/Cancelled
HAYES MICROCOMPUTER PRODUCTS, INC.
1986-06-17

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