Device 300397 Putty
K-Number: K241802 · 2024-11-08
ApplicantGeistlich Pharma AG
Decision Date2024-11-08
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Device 300397 Putty is a medical device manufactured by Geistlich Pharma AG. It received FDA 510(k) clearance on 2024-11-08 under approval number K241802. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Device 300397 Putty?
Device 300397 Putty is a medical device that received FDA 510(k) clearance on 2024-11-08. It is manufactured by Geistlich Pharma AG. The 510(k) number is K241802.
When was Device 300397 Putty approved by the FDA?
Device 300397 Putty received FDA 510(k) clearance on 2024-11-08, under approval number K241802.
What company makes Device 300397 Putty?
Device 300397 Putty is manufactured by Geistlich Pharma AG.
What is the FDA product code for Device 300397 Putty?
The FDA product code for Device 300397 Putty is MQV.
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K190754Orthoss(R)
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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.