92-09010

GUDID 07613327504958

MP CHIN PLATE

Stryker Leibinger GmbH & Co. KG

Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized Craniofacial fixation plate, non-bioabsorbable, non-customized
Primary Device ID07613327504958
NIH Device Record Keyd8af7212-7360-42dd-b225-da55f0a1a24e
Commercial Distribution StatusIn Commercial Distribution
Version Model Number92-09010
Catalog Number92-09010
Company DUNS316153956
Company NameStryker Leibinger GmbH & Co. KG
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS107613327504958 [Primary]

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


[07613327504958]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-02-05
Device Publish Date2019-11-22

Devices Manufactured by Stryker Leibinger GmbH & Co. KG

07613327556285 - NA2024-02-27 Facial iD MF 1 Mesh
07613327556308 - NA2024-02-23 Facial iD MF 2 meshes
07613327556322 - NA2024-02-23 Facial iD MF 3 meshes
07613327556346 - NA2024-02-23 Facial iD MF 4 meshes
07613327556377 - NA2024-02-23 Facial iD MF 5 meshes
07613327556391 - NA2024-02-23 Facial iD MF 6 meshes
07613327556827 - NA2024-02-23 Facial iD MF 1 mesh kit
07613327556834 - NA2024-02-23 Facial iD MF 3 meshes kit

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