SKYLINE 186803060S

GUDID 10705034412122

SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 60mm

Medos International Sàrl

Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile Bone-screw internal spinal fixation system, sterile
Primary Device ID10705034412122
NIH Device Record Keyc0afadb4-98d8-4e70-820b-02e8a88774c5
Commercial Distribution StatusIn Commercial Distribution
Brand NameSKYLINE
Version Model Number186803060S
Catalog Number186803060S
Company DUNS482661753
Company NameMedos International Sàrl
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

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034412122 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAppliance, fixation, spinal intervertebral body

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-14
Device Publish Date2021-06-05

On-Brand Devices [SKYLINE]

10705034412276SKYLINE ANTERIOR CERVICAL PLATE SYSTEM FIVE LEVEL PLATE 80mm
10705034412269SKYLINE ANTERIOR CERVICAL PLATE SYSTEM FIVE LEVEL PLATE 75mm
10705034412146SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 66mm
10705034412139SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 63mm
10705034412122SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 60mm
10705034412030SKYLINE ANTERIOR CERVICAL PLATE SYSTEM TWO LEVEL PLATE 44mm
10705034412023SKYLINE ANTERIOR CERVICAL PLATE SYSTEM TWO LEVEL PLATE 42mm
10705034412016SKYLINE ANTERIOR CERVICAL PLATE SYSTEM TWO LEVEL PLATE 40mm
10705034411927SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 30mm
10705034411910SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 28mm
10705034411903SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 26mm
10705034411897SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 24mm
10705034411880SKYLINE ANTERIOR CERVICAL PLATE SYSTEM ONE LEVEL PLATE 22mm
10705034412641SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW 4.5 x 18 mm
10705034412634SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW 4.5 x 16 mm
10705034412627SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW 4.5 x 14 mm
10705034412528SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 18mm
10705034412504SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 16mm
10705034412481SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 14mm
10705034412467SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 12mm
10705034412412SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm
10705034412399SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 16mm
10705034412375SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 14mm
10705034412351SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 12mm
10705034412115SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 57mm
10705034412108SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 54mm
10705034412092SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 51mm
10705034412085SKYLINE ANTERIOR CERVICAL PLATE SYSTEM THREE LEVEL PLATE 48mm
10705034215457SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CAM TIGHTENER SHAFT
10705034215426SKYLINE ANTERIOR CERVICAL PLATE SYSTEM EXPANSION TIP SCREWDRIVER

Trademark Results [SKYLINE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SKYLINE
SKYLINE
98419953 not registered Live/Pending
ZKH INDUSTRIAL SUPPLY CO., LTD.
2024-02-25
SKYLINE
SKYLINE
98307887 not registered Live/Pending
MARBLE SYSTEMS, INC.
2023-12-11
SKYLINE
SKYLINE
98279979 not registered Live/Pending
Niche Private Label LLC
2023-11-21
SKYLINE
SKYLINE
98223646 not registered Live/Pending
Kai U.S.A., Ltd.
2023-10-13
SKYLINE
SKYLINE
98088132 not registered Live/Pending
Skeptic Distillery Co.
2023-07-17
SKYLINE
SKYLINE
97800431 not registered Live/Pending
Nissan Jidosha Kabushiki Kaisha
2023-02-17
SKYLINE
SKYLINE
97789345 not registered Live/Pending
Nissan Jidosha Kabushiki Kaisha
2023-02-10
SKYLINE
SKYLINE
97650308 not registered Live/Pending
Nissan Jidosha Kabushiki Kaisha
2022-10-27
SKYLINE
SKYLINE
97589100 not registered Live/Pending
Insomniac Holdings, LLC
2022-09-13
SKYLINE
SKYLINE
97444068 not registered Live/Pending
Surfaces Southeast, LLC
2022-06-06
SKYLINE
SKYLINE
97306009 not registered Live/Pending
Othram, Inc.
2022-03-10
SKYLINE
SKYLINE
97051706 not registered Live/Pending
SV digital
2021-09-29

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