1-Level Cervical Plates, 22 mm

GUDID M739CP300220

CAPTIVA SPINE, INC.

Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable

Primary Device ID	M739CP300220
NIH Device Record Key	4c03343a-14a5-4ee0-a739-e3eaec661f0c
Commercial Distribution Status	In Commercial Distribution
Brand Name	1-Level Cervical Plates, 22 mm
Version Model Number	CP30022
Company DUNS	836975784
Company Name	CAPTIVA SPINE, INC.
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 Identifiers

Device Issuing Agency	Device ID
HIBCC	M739CP300220 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K141332

FDA Product Code

KWQ	Appliance, Fixation, Spinal Intervertebral Body