Medical Device Manufacturer · US , Timonium , MD

Osteo-Technology Intl., Inc. - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 1993
3
Total
2
Cleared
0
Denied

Osteo-Technology Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in Timonium, US.

Historical record: 2 cleared submissions from 1993 to 1995. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Osteo-Technology Intl., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Osteo-Technology Intl., Inc.
3 devices
1-3 of 3
Cleared Aug 07, 1995
REPLICA TOTAL HIP SYSTEM
K951741 · LPH
Orthopedic · 129d
Cleared Mar 07, 1994
BIOMETRIC TOTAL HIP SYSTEM
K935012 · JDI
Orthopedic · 138d
Cleared Jul 13, 1993
OTI EUROPEAN COMPRESSION SYSTEM
K925571 · HRS
Orthopedic · 252d
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All3 Orthopedic 3