8963S

GUDID 10845854016121

CANNULATED INTERFERENCE SCREW WITH GUIDEWIRE 9MM X 35MM

Conmed Corporation

Orthopaedic bone screw, non-bioabsorbable, sterile
Primary Device ID10845854016121
NIH Device Record Key56df5344-d16b-440d-929a-45fb35d1f912
Commercial Distribution Discontinuation2022-06-07
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number8963S
Catalog Number8963S
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(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM

Device Dimensions

Length35 Millimeter
Outer Diameter9 Millimeter
Length35 Millimeter
Outer Diameter9 Millimeter
Length35 Millimeter
Outer Diameter9 Millimeter
Length35 Millimeter
Outer Diameter9 Millimeter
Length35 Millimeter
Outer Diameter9 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854016121 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-06-08
Device Publish Date2015-10-24

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