MFG-05
K-Number: K230780 · 2023-10-05
ApplicantZimmer Medizinsysteme GmbH
Decision Date2023-10-05
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
MFG-05 is a medical device manufactured by Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2023-10-05 under approval number K230780. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MFG-05?
MFG-05 is a medical device that received FDA 510(k) clearance on 2023-10-05. It is manufactured by Zimmer Medizinsysteme GmbH. The 510(k) number is K230780.
When was MFG-05 approved by the FDA?
MFG-05 received FDA 510(k) clearance on 2023-10-05, under approval number K230780.
What company makes MFG-05?
MFG-05 is manufactured by Zimmer Medizinsysteme GmbH.
What is the FDA product code for MFG-05?
The FDA product code for MFG-05 is KPI.
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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.