DELTA XTENDTM 299966957

GUDID 10603295548935

DELTA XTENDTM MAKE TO ORDER LOCKING AO SCREWDRIVER SHAFT

DEPUY ORTHOPAEDICS, INC.

Surgical screwdriver, reusable
Primary Device ID10603295548935
NIH Device Record Keye3d8f359-9676-4ad1-a75a-894baf8774af
Commercial Distribution StatusIn Commercial Distribution
Brand NameDELTA XTENDTM
Version Model Number2999-66-957
Catalog Number299966957
Company DUNS080506581
Company NameDEPUY ORTHOPAEDICS, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110603295548935 [Primary]

FDA Product Code

KIJInstrument, surgical, orthopedic, dc-powered motor and accessory/attachment

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


[10603295548935]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-01
Device Publish Date2024-06-21

Devices Manufactured by DEPUY ORTHOPAEDICS, INC.

10603295554974 - EMPHASYS2026-02-12 EMPHASYS MAKE TO ORDER CUP IMPACTOR WITH STRIKE PLATE 14.5 INCH
10603295080121 - AML EXCEL2026-02-09 AML EXCEL FEMORAL/HUMERAL HEAD IMPACTOR
10603295082408 - DURALOC2026-02-09 DURALOC POLY IMPACTOR HANDLE
10603295083382 - SIGMA2026-02-09 SIGMA HP PARTIAL KNEE-UNI FEMORAL IMPACTOR
10603295084075 - SIGMA2026-02-09 SIGMA HP PARTIAL KNEE-TROCHLEA IMPACTOR
10603295088042 - GLOBAL FX2026-02-09 GLOBAL FX HEAD IMPACTION STAND
10603295090540 - GLOBAL AP2026-02-09 GLOBAL AP TAPER IMPACTOR
10603295090687 - GLOBAL AP2026-02-09 GLOBAL AP HEAD IMPACTOR

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.