Medical Device Manufacturer · US , New York , NY

Overture Resurfacing, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Overture Resurfacing, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Overture Resurfacing, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Cor Medical Ventures, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Overture Resurfacing, Inc.
2 devices
1-2 of 2
Cleared Jul 07, 2023
Overture Orthopaedics Patellofemoral System
K231253 · KRR
Orthopedic · 67d
Cleared Mar 10, 2023
Uni Knee Resurfacing System
K221292 · HSX
Orthopedic · 310d
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