92-15905

GUDID 37613154131847

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 ID37613154131847
NIH Device Record Keyb061f66e-6464-49bb-9c10-5000461871ae
Commercial Distribution StatusIn Commercial Distribution
Version Model Number92-15905
Catalog Number92-15905
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

Length5 Millimeter
Length5 Millimeter
Length5 Millimeter
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter
Device Size Text, specify0
Length5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613154131846 [Unit of Use]
GS137613154131847 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

Moist Heat or Steam Sterilization


[37613154131847]

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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