Cannulated Screws SU 0913-00-2

GUDID 04042409088483

Washer, I-ø8.5, O-ø13.0 Titanium

aap Implantate AG

Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Orthopaedic bone washer, non-sterile Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer Implantable bone washer

Primary Device ID	04042409088483
NIH Device Record Key	f0adc849-23f4-4854-89f9-b63d9acb12e5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Cannulated Screws
Version Model Number	SU 0913-00-2
Catalog Number	SU 0913-00-2
Company DUNS	328420633
Company Name	aap Implantate AG
Device Count	5
DM Exempt	true
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	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 Identifiers

Device Issuing Agency	Device ID
GS1	04042409088483 [Primary]
GS1	04042409438929 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K990776

FDA Product Code

HTN	Washer, Bolt Nut