510(k) K241802

Device
Device 300397 Putty
Applicant
Geistlich Pharma AG
510(k) number
K241802
Product code
MQV
Decision
Substantially Equivalent (SESE)
Decision date
2024-11-08
Date received
2024-06-21
Regulation
888.3045
Classification name
Filler, Bone Void, Calcium Compound
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Marco Steiner
Address
Bahnhofstrasse 40 Wolhusen CH 6110 6110

FDA Registration Numbers

Source Documents

510(k) summary PDF

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