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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Geistlich Pharma AG. It received FDA 510(k) clearance on 2024-11-08 under 510(k) 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. The listed applicant is Geistlich Pharma AG. The 510(k) number is K241802.

When did Device 300397 Putty receive FDA 510(k) clearance?

Device 300397 Putty received FDA 510(k) clearance on 2024-11-08, under 510(k) number K241802.

Who is the listed applicant for Device 300397 Putty?

The FDA 510(k) record lists Geistlich Pharma AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Device 300397 Putty?

The FDA product code for Device 300397 Putty is MQV.

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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.

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