FusionFrame Ring Lock System
K-Number: K200343 · 2020-09-14
Device Summary
Frequently Asked Questions
What is the FusionFrame Ring Lock System?
FusionFrame Ring Lock System is a medical device that received FDA 510(k) clearance on 2020-09-14. The listed applicant is Glw Medical Innovation. The 510(k) number is K200343.
When did FusionFrame Ring Lock System receive FDA 510(k) clearance?
FusionFrame Ring Lock System received FDA 510(k) clearance on 2020-09-14, under 510(k) number K200343.
Who is the listed applicant for FusionFrame Ring Lock System?
The FDA 510(k) record lists Glw Medical Innovation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FusionFrame Ring Lock System?
The FDA product code for FusionFrame Ring Lock System is KTT.
Related Devices (Code: KTT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.