510(k) K241753

Device
Immediate Molar Implants
Applicant
Biomet 3i, LLC
510(k) number
K241753
Product code
DZE
Decision
Substantially Equivalent (SESE)
Decision date
2024-10-23
Date received
2024-06-18
Regulation
872.3640
Classification name
Implant, Endosseous, Root-Form
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Krupal Patel
Address
4555 Riverside Dr. Palm Beach Gardens FL US 33410 33410

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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