Stable-L™

GUDID B6788250310

Stable-L Trial, 36x28x16, 6 deg

NEXUS SPINE, L.L.C.

Spinal implant trial

Primary Device ID	B6788250310
NIH Device Record Key	56b53848-9a5e-47b8-a54a-56ecb33c8d09
Commercial Distribution Status	In Commercial Distribution
Brand Name	Stable-L™
Version Model Number	825031
Company DUNS	028137605
Company Name	NEXUS SPINE, L.L.C.
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 Dimensions

Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter
Height	16 Millimeter
Width	36 Millimeter
Length	28 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B678825031 [Direct Marking]
HIBCC	B6788250310 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K212498

FDA Product Code

HWT	Template
LXH	Orthopedic Manual Surgical Instrument