FusionFrame Ring Lock System
K-Number: K200343 · 2020-09-14
ApplicantGlw Medical Innovation
Decision Date2020-09-14
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
FusionFrame Ring Lock System is a medical device manufactured by Glw Medical Innovation. It received FDA 510(k) clearance on 2020-09-14 under approval number K200343. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Glw Medical Innovation. The 510(k) number is K200343.
When was FusionFrame Ring Lock System approved by the FDA?
FusionFrame Ring Lock System received FDA 510(k) clearance on 2020-09-14, under approval number K200343.
What company makes FusionFrame Ring Lock System?
FusionFrame Ring Lock System is manufactured by Glw Medical Innovation.
What is the FDA product code for FusionFrame Ring Lock System?
The FDA product code for FusionFrame Ring Lock System is KTT.
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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.