101140030

GUDID 10603295000440

SELF TAPPING ROOF PILE SCREW 30mm

DEPUY ORTHOPAEDICS, INC.

Orthopaedic bone screw (non-sliding)
Primary Device ID10603295000440
NIH Device Record Key4d30255f-fc26-43e8-bd27-4abb187ee5f1
Commercial Distribution StatusIn Commercial Distribution
Version Model Number1011-40-030
Catalog Number101140030
Company DUNS080506581
Company NameDEPUY ORTHOPAEDICS, INC.
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
GS110603295000440 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDJMesh, surgical, acetabular, hip, prosthesis

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-10-27
Device Publish Date2015-09-24

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

10603295086918 - NA2024-11-07 REAMER HOLE GAUGE
10603295216742 - P.F.C.2024-11-07 P.F.C. UNIVERSAL MODULAR STEM WRENCH
10603295227304 - SIGMA LCS HIGH PERFORMANCE2024-11-07 SIGMA LCS HIGH PERFORMANCE MBT KEEL PUNCH CEMENTED SIZE 1-1.5
10603295227311 - SIGMA LCS HIGH PERFORMANCE2024-11-07 SIGMA LCS HIGH PERFORMANCE MBT KEEL PUNCH CEMENTED SIZE 2-3
10603295227328 - SIGMA LCS HIGH PERFORMANCE2024-11-07 SIGMA LCS HIGH PERFORMANCE MBT KEEL PUNCH CEMENTED SIZE 4-7
10603295227335 - SIGMA LCS HIGH PERFORMANCE2024-11-07 SIGMA LCS HIGH PERFORMANCE MBT KEEL PUNCH NONCEMENTED SIZE 1-1.5
10603295227342 - SIGMA LCS HIGH PERFORMANCE2024-11-07 SIGMA LCS HIGH PERFORMANCE MBT KEEL PUNCH NONCEMENTED SIZE 2-3
10603295227359 - SIGMA LCS HIGH PERFORMANCE2024-11-07 SIGMA LCS HIGH PERFORMANCE MBT KEEL PUNCH NONCEMENTED SIZE 4-7

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