474912S

GUDID H679474912S0

120 DEG TI LOCKING SLV-STERILE F/13-15 TI CANN FEMORAL NAILS

SYNTHES (U.S.A.) LP

Orthopaedic fixation plate, non-bioabsorbable, sterile Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable
Primary Device IDH679474912S0
NIH Device Record Key33f1e326-2412-49be-82b3-3e03143f5aa2
Commercial Distribution Discontinuation2019-10-12
Commercial Distribution StatusIn Commercial Distribution
Version Model Number474.912S
Catalog Number474912S
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982234353 [Primary]
HIBCCH679474912S0 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDNIMPLANT, FIXATION DEVICE, SPINAL

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


[H679474912S0]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-09-19
Device Publish Date2015-09-14

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

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H679022221140 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/14MM
H679022221160 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/16MM
H679022221180 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/18MM
H679022221200 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/20MM
H679022221220 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/22MM
H679022221240 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/24MM
H679022221260 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/26MM

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