FDA Registration Active 🇺🇸 United States

Duo Lumbar Interbody Fusion Device

Reg #: 2135156 · FEI: 3003179719 · Expires 2025
Products
1
Proprietary Names
1
Establishment Types
1
Classifications
1

Registration Details

Registration Name
SPINEOLOGY INC.
Registration Number
2135156
FEI Number
3003179719
Status
Active
Expiry Year
2025
Initial Importer
No
Address
7800 THIRD STREET N., SUITE 600
City
Saint Paul
State
MN
ZIP
55128
Country
US

Regulatory Submissions

510(k) Number
K181792

Owner / Operator

Firm Name
Spineology Inc
Operator Number
9036813
Address
7800 Third ST. N., Suite 600
City
Saint Paul
State
MN
Postal Code
55128
Country
US

Products

Device Name Product Code
Intervertebral Fusion Device With Bone Graft, Lumbar MAX

Proprietary Names

Duo Lumbar Interbody Fusion Device

Establishment Types

Manufacture Medical Device