Plus Orthopedics - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Plus Orthopedics has 38 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.
Historical record: 38 cleared submissions from 1997 to 2004.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
38 devices
Cleared
Jan 08, 2004
PROMOS SHOULDER
Orthopedic
182d
Cleared
Dec 18, 2003
MODIFICATION TO SLIM GLIDING NAIL SYSTEM
Orthopedic
16d
Cleared
Sep 23, 2003
MODULAR PLUS HIP STEM
Orthopedic
21d
Cleared
Sep 10, 2003
IP-XS COMPRESSION NAIL SYSTEM
Orthopedic
23d
Cleared
Aug 08, 2003
VKS/TC-PLUS REVISION KNEE
Orthopedic
18d
Cleared
Jul 25, 2003
UC-PLUS SOLUTION UNICONDYLAR KNEE
Orthopedic
23d
Cleared
Jun 06, 2003
PLUS ORTHOPEDICS CEMENTED HIP STEM
Orthopedic
53d
Cleared
Apr 24, 2003
MODIFICATION TO MODULAR PLUS REVISION STEM
Orthopedic
27d
Cleared
Jan 15, 2003
UNI HIP STEM
Orthopedic
30d
Cleared
Dec 24, 2002
RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE
Orthopedic
54d
Cleared
Nov 08, 2002
MODIFICATION TO VKS KNEE SYSTEM
Orthopedic
28d
Cleared
Oct 18, 2002
VKS KNEE SYSTEM
Orthopedic
105d
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