C8952

GUDID 20845854016463

8MM X 30MM CANNULATED INTERFERENCE SCREW WITH GUIDEWIRE

Conmed Corporation

Orthopaedic bone screw, non-bioabsorbable, sterile
Primary Device ID20845854016463
NIH Device Record Key259a2cdd-3e20-410d-823e-d3d288024a65
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberC8952
Catalog NumberC8952
Company DUNS071595540
Company NameConmed Corporation
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)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com

Device Dimensions

Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter
Length30 Millimeter
Outer Diameter8 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS120845854016463 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


[20845854016463]

Radiation Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

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