Cross Connector, Medium

GUDID M73924713752

Cross Connector, Medium

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	M73924713752
NIH Device Record Key	2fd82dc7-956a-4413-908e-fe36d1ffdc49
Commercial Distribution Discontinuation	2017-08-08
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Cross Connector, Medium
Version Model Number	2471-3752
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	M73924713752 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K131538

FDA Product Code

MNI	Orthosis, Spinal Pedicle Fixation