PTG-05
K-Number: K240347 · 2024-07-21
ApplicantZimmer Medizinsysteme GmbH
Decision Date2024-07-21
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
PTG-05 is a medical device manufactured by Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2024-07-21 under approval number K240347. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the PTG-05?
PTG-05 is a medical device that received FDA 510(k) clearance on 2024-07-21. It is manufactured by Zimmer Medizinsysteme GmbH. The 510(k) number is K240347.
When was PTG-05 approved by the FDA?
PTG-05 received FDA 510(k) clearance on 2024-07-21, under approval number K240347.
What company makes PTG-05?
PTG-05 is manufactured by Zimmer Medizinsysteme GmbH.
What is the FDA product code for PTG-05?
The FDA product code for PTG-05 is NGX.
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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.