Medical Device Manufacturer · US , Mountain View , CA

Advanced Osseous Technologies - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990
2
Total
2
Cleared
0
Denied

Advanced Osseous Technologies has 2 FDA 510(k) cleared medical devices. Based in Mountain View, US.

Historical record: 2 cleared submissions from 1990 to 1991. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Advanced Osseous Technologies Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Advanced Osseous Technologies
2 devices
1-2 of 2
Cleared Mar 05, 1991
SYSTEM TEN, MODEL 100 SURGERY SYST/ORTHOPAEDIC USE
K905451 · JDX
Orthopedic · 90d
Cleared Mar 16, 1990
SYSTEM TEN MODEL 100 SURGICAL SYSTEM
K900003 · JDX
Orthopedic · 73d
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