510(k) K220049

Device
Optimotion Implants Porous Metal-Backed Patella
Applicant
Optimotion Implants, LLC
510(k) number
K220049
Product code
MBH
Decision
Substantially Equivalent (SESE)
Decision date
2022-03-14
Date received
2022-01-06
Regulation
888.3565
Classification name
Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Andy Rynearson
Address
6052 Turkey Lake Rd. Orlando FL US 32819 32819

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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K242543Persona the Personalized Knee System (Persona Ti-Nidium PPS Femurs)Zimmer, Inc.2024-11-22