510(k) K242050

Device
Montage Settable Bone Putty
Applicant
Orthocon, Inc.
510(k) number
K242050
Product code
MQV
Decision
Substantially Equivalent (SESE)
Decision date
2024-07-29
Date received
2024-07-12
Regulation
888.3045
Classification name
Filler, Bone Void, Calcium Compound
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Aniq Darr
Address
700 Fairfield Ave., Suite 1 Stamford CT US 10533 10533

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code MQV

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