Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by Vito Lore
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172484
08/17/2017
A-CIFT SoloFuse
SpineFrontier, Inc.
K232605
08/28/2023
Sacrix« Sacroiliac Joint Fusion Device System, Inspan« ScrewLES Fusion System, Invue« MAXÖ + Invue Inset Anterior Cervical Plate System, and FacetFuse« Screw Fixation System
LESspine Innovations
K193106
11/08/2019
SpineFrontier Lumbar Interbody Fusion Device System
SpineFrontier, Inc.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact