Plate Holder

GUDID 09348215066918

SIGNATURE ORTHOPAEDICS PTY LTD

Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

Primary Device ID	09348215066918
NIH Device Record Key	1fddcf08-b889-41f9-b5a7-0ccd76ca9fc9
Commercial Distribution Status	In Commercial Distribution
Brand Name	Plate Holder
Version Model Number	132-16-0016
Company DUNS	751993028
Company Name	SIGNATURE ORTHOPAEDICS PTY LTD
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	false
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 Identifiers

Device Issuing Agency	Device ID
GS1	09348215066918 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K163625

FDA Product Code

KWQ	Appliance, Fixation, Spinal Intervertebral Body