52-20412

GUDID 34546540355622

Bone Screws, Cross-Pin

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 ID34546540355622
NIH Device Record Key4348640e-de8f-4a2e-a505-cc619ae591ca
Commercial Distribution StatusIn Commercial Distribution
Version Model Number52-20412
Catalog Number52-20412
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

Length12 Millimeter
Length12 Millimeter
Length12 Millimeter
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter
Device Size Text, specify0
Length12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540355621 [Unit of Use]
GS134546540355622 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


[34546540355622]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-07-01
Device Publish Date2015-06-16

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