Encore Orthopedics, Inc. - FDA 510(k) Cleared Devices
85
Total
74
Cleared
0
Denied
Encore Orthopedics, Inc. has 74 FDA 510(k) cleared orthopedic devices. Based in Red Rock, US.
Historical record: 74 cleared submissions from 1993 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.
85 devices
Cleared
Jul 06, 2004
3DKNEE POROUS COATED FEMORAL COMPONENT
Orthopedic
293d
Cleared
Jul 12, 2002
3D KNEE
Orthopedic
182d
Cleared
Jun 04, 2002
UNICONDYLAR KNEE
Orthopedic
90d
Cleared
Feb 14, 2002
MODIFICATION TO PASS SPINAL SYSTEM
Orthopedic
22d
Cleared
Feb 11, 2002
KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP
Orthopedic
25d
Cleared
Jan 17, 2002
CEMENTED CALCAR HIP SYSTEM
Orthopedic
87d
Cleared
Jan 15, 2002
PASS SPINAL SYSTEM
Orthopedic
90d
Cleared
Dec 06, 2001
PLASMA SPRAYED SHOULDER
Orthopedic
408d
Cleared
Nov 15, 2001
PASS SPINAL SYSTEM
Orthopedic
30d
Cleared
Oct 24, 2001
PASS SPINAL SYSTEM
Orthopedic
30d
Cleared
Aug 22, 2001
RADIOGRAPHIC MARKERS
General & Plastic Surgery
70d
Cleared
Jul 31, 2001
PASS SPINAL SYSTEM
Orthopedic
19d
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