CONTACT® ALP Anterior Lumbar Plate System

GUDID 00846468028879

PUSH STYLE TEMPORARY HOLDING PIN

Pioneer Surgical Technology, Inc.

General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit
Primary Device ID00846468028879
NIH Device Record Keyebc33224-f2e5-4118-a671-b19f88b5597a
Commercial Distribution Discontinuation2018-09-19
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCONTACT® ALP Anterior Lumbar Plate System
Version Model Number25-PUSHPIN-27
Company DUNS793384496
Company NamePioneer Surgical Technology, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100846468028879 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


[00846468028879]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-09-20
Device Publish Date2016-09-30

On-Brand Devices [CONTACT® ALP Anterior Lumbar Plate System]

00846468029029TEMPORARY HOLDING PIN, THREADED
0084646802897846mm ANTERIOR SACRAL PLATE
0084646802896144mm ANTERIOR SACRAL PLATE
0084646802895442mm ANTERIOR SACRAL PLATE
0084646802894740mm ANTERIOR SACRAL PLATE
0084646802893038mm ANTERIOR SACRAL PLATE
0084646802892336mm ANTERIOR SACRAL PLATE
0084646802891634mm ANTERIOR SACRAL PLATE
00846468028886T-HANDLE, RATCHETING
00846468028879PUSH STYLE TEMPORARY HOLDING PIN
0084646802878746mm ANTERIOR LUMBAR PLATE
0084646802877044mm ANTERIOR LUMBAR PLATE
0084646802876342mm ANTERIOR LUMBAR PLATE
0084646802875640mm ANTERIOR LUMBAR PLATE
0084646802874938mm ANTERIOR LUMBAR PLATE
0084646802873236mm ANTERIOR LUMBAR PLATE
0084646802872534mm ANTERIOR LUMBAR PLATE
00846468028633AUXILIARY PLATE AND SCREW CADDY
008464680286266.5 x 40 RESCUE SCREW ASSEMBLY
008464680286196.5 x 38 RESCUE SCREW ASSEMBLY
008464680286026.5 x 36 RESCUE SCREW ASSEMBLY
008464680285966.5 x 34 RESCUE SCREW ASSEMBLY
008464680285896.5 x 32 RESCUE SCREW ASSEMBLY
008464680285726.5 x 30 RESCUE SCREW ASSEMBLY
008464680285656.5 x 28 RESCUE SCREW ASSEMBLY
008464680285586.5 x 26 RESCUE SCREW ASSEMBLY
008464680285416.5 x 24 RESCUE SCREW ASSEMBLY
008464680285346.5 x 22 RESCUE SCREW ASSEMBLY
008464680285276.0 x 40 LUMBAR SCREW ASSEMBLY
008464680285106.0 x 38 LUMBAR SCREW ASSEMBLY
008464680285036.0 x 36 LUMBAR SCREW ASSEMBLY
008464680284976.0 x 34 LUMBAR SCREW ASSEMBLY
008464680284806.0 x 32 LUMBAR SCREW ASSEMBLY
008464680284736.0 x 30 LUMBAR SCREW ASSEMBLY
008464680284666.0 x 28 LUMBAR SCREW ASSEMBLY
008464680284596.0 x 26 LUMBAR SCREW ASSEMBLY
008464680284426.0 x 24 LUMBAR SCREW ASSEMBLY
008464680284356.0 x 22 LUMBAR SCREW ASSEMBLY

Trademark Results [CONTACT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CONTACT
CONTACT
97749208 not registered Live/Pending
Contact Wearables LLC
2023-01-10
CONTACT
CONTACT
97391779 not registered Live/Pending
Immerse Yourself Entertainment
2022-05-02
CONTACT
CONTACT
88481644 5897359 Live/Registered
CNS OUTDOOR TECHNOLOGIES, LLC
2019-06-20
CONTACT
CONTACT
88319862 not registered Live/Pending
Antowne K. Clower
2019-02-28
CONTACT
CONTACT
88300050 5901163 Live/Registered
Play'n GO Marks Ltd.
2019-02-13
CONTACT
CONTACT
87841036 not registered Dead/Abandoned
Orsmond, Albert N.
2018-03-20
CONTACT
CONTACT
86902846 not registered Dead/Abandoned
Pling, Ali Ibrahim
2016-02-09
CONTACT
CONTACT
86902844 5045013 Live/Registered
Pling, Ali Ibrahim
2016-02-09
CONTACT
CONTACT
86754741 not registered Dead/Abandoned
NLU Products, L.L.C.
2015-09-11
CONTACT
CONTACT
86744575 5223848 Live/Registered
NLU Products, L.L.C.
2015-09-01
CONTACT
CONTACT
86685439 not registered Dead/Abandoned
This is Blueprint Management Ltd.
2015-07-07
CONTACT
CONTACT
86647224 not registered Dead/Abandoned
Edge-Works Manufacturing Company
2015-06-01

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