Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by GLW, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K221489
05/23/2022
Artemis Proximal Femoral Nail System
GLW, Inc.
K201379
05/26/2020
Artemis Proximal Femoral Nail System
GLW, Inc.
K223847
12/22/2022
CREEDÖ Cannulated Screws
GLW, Inc.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact