CORUS™ Allograft Delivery Instrument

GUDID 00852776006454

A manual orthopedic surgical instrument used to deliver structural bone graft to a target area of the spine. The Allograft Delivery Instrument is manufactured using medical grade polycarbonate resin and stainless steel. The CORUS™ Allograft Delivery Instrument is intended and indicated for the delivery of structural bone graft to a target area of the spine.

PROVIDENCE MEDICAL TECHNOLOGY, INC.

Bone graft syringe Bone graft syringe, single-use Bone graft syringe, single-use Bone graft syringe, single-use Bone graft syringe, single-use Bone graft syringe, single-use Bone graft syringe, single-use Bone graft syringe, single-use
Primary Device ID00852776006454
NIH Device Record Key0c57669b-d50b-40af-a21f-c29fabb991d5
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORUS™ Allograft Delivery Instrument
Version Model NumberPD-10-400
Company DUNS969820245
Company NamePROVIDENCE MEDICAL 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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com
Phone4153013128
Emailjmandrusov@providencemt.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100852776006454 [Primary]
GS110852776006451 [Package]
Package: [1 Units]
In Commercial Distribution

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-08-01
Device Publish Date2019-07-24

Devices Manufactured by PROVIDENCE MEDICAL TECHNOLOGY, INC.

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Trademark Results [CORUS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CORUS
CORUS
98033599 not registered Live/Pending
Corus Caribbean Holdings Ltd.
2023-06-08
CORUS
CORUS
98031511 not registered Live/Pending
Corus Caribbean Holdings Ltd.
2023-06-07
CORUS
CORUS
97426694 not registered Live/Pending
Careismatic Brands, Inc.
2022-05-24
CORUS
CORUS
90156790 not registered Live/Pending
Metropolitan Staple Corp.
2020-09-03
CORUS
CORUS
90080128 not registered Live/Pending
Health Catalyst, Inc.
2020-07-29
CORUS
CORUS
88831023 not registered Live/Pending
Corus International, Inc.
2020-03-11
CORUS
CORUS
88764426 not registered Live/Pending
Corus International, Inc.
2020-01-17
CORUS
CORUS
88687135 not registered Live/Pending
2195646 Alberta Inc.
2019-11-11
CORUS
CORUS
88277032 not registered Live/Pending
Providence Medical Technology, Inc.
2019-01-25
CORUS
CORUS
87952907 5858421 Live/Registered
Corus Entertainment Inc.
2018-06-07
CORUS
CORUS
87317721 not registered Dead/Abandoned
The Johns Hopkins University
2017-01-30
CORUS
CORUS
87144545 5249059 Live/Registered
Corus Dental Solutions, S.A.
2016-08-19

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