51-15904

GUDID 34546540393969

BONE SCREWS, CROSS-PIN, SELF-DRILLING

Stryker Leibinger GmbH & Co. KG

Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable, sterile Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable
Primary Device ID34546540393969
NIH Device Record Key3443d0c8-f958-4cc1-ab9f-c87c61ed3fdf
Commercial Distribution StatusIn Commercial Distribution
Version Model Number51-15904
Catalog Number51-15904
Company DUNS316153956
Company NameStryker Leibinger GmbH & Co. KG
Device Count5
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

Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter
Device Size Text, specify0
Length4 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540393968 [Unit of Use]
GS134546540393969 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


[34546540393969]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-06-16

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