Medical Device Manufacturer · US , Hunt Valley , MD

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

21 submissions · 20 cleared · Since 1996
21
Total
20
Cleared
0
Denied

Osteoimplant Technology, Inc. has 20 FDA 510(k) cleared orthopedic devices. Based in Hunt Valley, US.

Historical record: 20 cleared submissions from 1996 to 2005.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Osteoimplant Technology, Inc.
21 devices
1-12 of 21
Cleared Jan 25, 2005
Z - SERIES MODULAR TOTAL HIP SYSTEM PLASMA COATED
K040685 · LWJ
Orthopedic · 315d
Cleared Nov 16, 2004
OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
K041443 · LZO
Orthopedic · 168d
Cleared May 06, 2004
OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
K040225 · KWZ
Orthopedic · 94d
Cleared Dec 03, 2003
Z-SERIES MODULAR TOTAL HIP SYSTEM
K032729 · LPH
Orthopedic · 91d
Cleared Jun 12, 2003
OTI BONE CEMENT PLUG
K030608 · JDK
Orthopedic · 106d
Cleared Nov 20, 2002
OTI UNICONDULAR INTERPOSITIONAL SPACER
K022779 · HSH
Orthopedic · 90d
Cleared Jul 23, 2002
R120 MODULAR TOTAL HIP SYSTEM
K021822 · JDI
Orthopedic · 49d
Cleared Dec 11, 2001
MJS POSTERIOR STABILIZED KNEE SYSTEM
K012762 · HRY
Orthopedic · 116d
Cleared Sep 05, 2001
R120 MODULAR TOTAL HIP SYSTEM
K011774 · JDI
Orthopedic · 90d
Cleared Jan 19, 2001
OTI CERAMIC FEMORAL HEAD SYSTEM
K003316 · LZO
Orthopedic · 88d
Cleared Jan 10, 2001
TRIAD II MODULAR TOTAL HIP SYSTEM
K003199 · LPH
Orthopedic · 90d
Cleared Jun 08, 2000
OMEGA II MODULAR TOTAL HIP SYSTEM
K000817 · JDI
Orthopedic · 87d
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