Cross Connector, Large

GUDID M73924714975

Cross Connector, Large

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	M73924714975
NIH Device Record Key	42b4a2e1-9c94-435d-b53a-2e8fc5f926ae
Commercial Distribution Discontinuation	2017-08-08
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Cross Connector, Large
Version Model Number	2471-4975
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	M73924714975 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K131538

FDA Product Code

MNH	Orthosis, Spondylolisthesis Spinal Fixation