JARVIS Glenoid Reverse Shoulder Prosthesis
K-Number: K242253 · 2024-11-25
ApplicantFH Industrie
Decision Date2024-11-25
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
JARVIS Glenoid Reverse Shoulder Prosthesis is a medical device manufactured by FH Industrie. It received FDA 510(k) clearance on 2024-11-25 under approval number K242253. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the JARVIS Glenoid Reverse Shoulder Prosthesis?
JARVIS Glenoid Reverse Shoulder Prosthesis is a medical device that received FDA 510(k) clearance on 2024-11-25. It is manufactured by FH Industrie. The 510(k) number is K242253.
When was JARVIS Glenoid Reverse Shoulder Prosthesis approved by the FDA?
JARVIS Glenoid Reverse Shoulder Prosthesis received FDA 510(k) clearance on 2024-11-25, under approval number K242253.
What company makes JARVIS Glenoid Reverse Shoulder Prosthesis?
JARVIS Glenoid Reverse Shoulder Prosthesis is manufactured by FH Industrie.
What is the FDA product code for JARVIS Glenoid Reverse Shoulder Prosthesis?
The FDA product code for JARVIS Glenoid Reverse Shoulder Prosthesis is PHX.
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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.