ThermoPro
K-Number: K161862 · 2016-11-14
ApplicantZimmer Medizinsysteme GmbH
Decision Date2016-11-14
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
ThermoPro is a medical device manufactured by Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2016-11-14 under approval number K161862. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ThermoPro?
ThermoPro is a medical device that received FDA 510(k) clearance on 2016-11-14. It is manufactured by Zimmer Medizinsysteme GmbH. The 510(k) number is K161862.
When was ThermoPro approved by the FDA?
ThermoPro received FDA 510(k) clearance on 2016-11-14, under approval number K161862.
What company makes ThermoPro?
ThermoPro is manufactured by Zimmer Medizinsysteme GmbH.
What is the FDA product code for ThermoPro?
The FDA product code for ThermoPro is IMJ.
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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.