RFG-01
K-Number: K240178 · 2024-07-15
Device Summary
Frequently Asked Questions
What is the RFG-01?
RFG-01 is a medical device that received FDA 510(k) clearance on 2024-07-15. The listed applicant is Zimmer Medizinsysteme GmbH. The 510(k) number is K240178.
When did RFG-01 receive FDA 510(k) clearance?
RFG-01 received FDA 510(k) clearance on 2024-07-15, under 510(k) number K240178.
Who is the listed applicant for RFG-01?
The FDA 510(k) record lists Zimmer Medizinsysteme GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RFG-01?
The FDA product code for RFG-01 is PBX.
Other records listing Zimmer Medizinsysteme GmbH as applicant
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.
Related Devices (Code: PBX)
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.