MATTA 425755

GUDID 04546540413574

Straight Acetabular Plate

Stryker Trauma SA

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable Orthopaedic fixation plate, non-bioabsorbable

Primary Device ID	04546540413574
NIH Device Record Key	6bc6a481-3a0a-4fd3-9cc1-6aea1cb7cfbc
Commercial Distribution Status	In Commercial Distribution
Brand Name	MATTA
Version Model Number	425755
Catalog Number	425755
Company DUNS	481999654
Company Name	Stryker Trauma SA
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
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

Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0
Length	58.5 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540413574 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K001614

FDA Product Code

KTW	APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, SINGLE COMPONENT