EZYPOR
K-Number: K212741 · 2022-06-24
Decision Date2022-06-24
Product CodeHPZ
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
EZYPOR is a medical device manufactured by Fci (France Chirurgie Instrumentation) Sas. It received FDA 510(k) clearance on 2022-06-24 under approval number K212741. The device is classified under product code HPZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EZYPOR?
EZYPOR is a medical device that received FDA 510(k) clearance on 2022-06-24. It is manufactured by Fci (France Chirurgie Instrumentation) Sas. The 510(k) number is K212741.
When was EZYPOR approved by the FDA?
EZYPOR received FDA 510(k) clearance on 2022-06-24, under approval number K212741.
What company makes EZYPOR?
EZYPOR is manufactured by Fci (France Chirurgie Instrumentation) Sas.
What is the FDA product code for EZYPOR?
The FDA product code for EZYPOR is HPZ.
Other Devices by Fci (France Chirurgie Instrumentation) Sas
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.