SD391931

GUDID 10886982311535

TIGHTENING CAP ASSEMBLY K-WIRE CUTTER

SYNTHES (U.S.A.) LP

Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter Orthopaedic implantable-device cutter
Primary Device ID10886982311535
NIH Device Record Key67e6b025-ab4d-4fdd-8a22-09865411f8e2
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberSD391.931
Catalog NumberSD391931
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982311535 [Primary]

FDA Product Code

HXZCUTTER, WIRE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


[10886982311535]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-06
Device Publish Date2024-05-29

Devices Manufactured by SYNTHES (U.S.A.) LP

H981023060100 - NA2024-07-12 6.0MM PELVIC ROD-LEFT
H981023060120 - NA2024-07-12 6.0MM PELVIC ROD-RIGHT
H981042006140 - Axon2024-07-12 3.5MM TI CANCELLOUS AXON(TM) SCREW 28MM THREAD LENGTH
H981042006150 - Axon2024-07-12 3.5MM TI CANCELLOUS AXON(TM) SCREW 30MM THREAD LENGTH
H981042006160 - Axon2024-07-12 3.5MM TI CANCELLOUS AXON(TM) SCREW 32MM THREAD LENGTH
H981042006170 - Axon2024-07-12 3.5MM TI CANCELLOUS AXON(TM) SCREW 34MM THREAD LENGTH
H981042006180 - Axon2024-07-12 3.5MM TI CANCELLOUS AXON(TM) SCREW 36MM THREAD LENGTH
H981042006190 - Axon2024-07-12 3.5MM TI CANCELLOUS AXON(TM) SCREW 38MM THREAD LENGTH

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