56-90312

GUDID 07613327122954

1,5/1,7MM DYNAMIC MESH-MALL-SMALL

Stryker Leibinger GmbH & Co. KG

Craniofacial fixation plate, non-bioabsorbable

Primary Device ID	07613327122954
NIH Device Record Key	bc6f323a-2d44-488a-b1c4-0aa20c39fbc3
Commercial Distribution Status	In Commercial Distribution
Version Model Number	56-90312
Catalog Number	56-90312
Company DUNS	316153956
Company Name	Stryker Leibinger GmbH & Co. KG
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter
Device Size Text, specify	0
Length	40 Millimeter
Width	40 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327122954 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K161821

FDA Product Code

GWO	Plate, cranioplasty, preformed, alterable