9mm Trial Cage 11

GUDID 09348215067519

SIGNATURE ORTHOPAEDICS PTY LTD

Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable

Primary Device ID	09348215067519
NIH Device Record Key	321e7200-ac26-406a-9da9-cec2f593cecc
Commercial Distribution Status	In Commercial Distribution
Brand Name	9mm Trial Cage 11
Version Model Number	132-072-129
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	09348215067519 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K172020

FDA Product Code

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar