RFG-01
K-Number: K240178 · 2024-07-15
ApplicantZimmer Medizinsysteme GmbH
Decision Date2024-07-15
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
RFG-01 is a medical device manufactured by Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2024-07-15 under approval number K240178. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RFG-01?
RFG-01 is a medical device that received FDA 510(k) clearance on 2024-07-15. It is manufactured by Zimmer Medizinsysteme GmbH. The 510(k) number is K240178.
When was RFG-01 approved by the FDA?
RFG-01 received FDA 510(k) clearance on 2024-07-15, under approval number K240178.
What company makes RFG-01?
RFG-01 is manufactured by Zimmer Medizinsysteme GmbH.
What is the FDA product code for RFG-01?
The FDA product code for RFG-01 is PBX.
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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.