Intermedics Orthopedics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intermedics Orthopedics - FDA 510(k) Cleared Devices
Recent clearances: NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI, NATURAL-KNEE II REVISION FEMORAL SPACER LUGS, NATURAL-HIP SYSTEM COCR REVISION STEM
108
Total
82
Cleared
0
Denied
Intermedics Orthopedics has 82 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 82 cleared submissions from 1982 to 1997.
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 - Intermedics Orthopedics
108 devices
Cleared
Jul 03, 1997
NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI
Orthopedic
160d
Cleared
Apr 30, 1997
NATURAL-KNEE II REVISION FEMORAL SPACER LUGS
Orthopedic
79d
Cleared
Apr 08, 1997
NATURAL-HIP SYSTEM COCR REVISION STEM
Orthopedic
82d
Cleared
Feb 27, 1997
SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDS
Orthopedic
14d
Cleared
Jan 27, 1997
NATURAL-HIP SYSTEM COCR STEM
Orthopedic
87d
Cleared
Jan 16, 1997
MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA
Orthopedic
77d
Cleared
Oct 28, 1996
PATELLOFEMORAL JOINT PROSTHESIS
Orthopedic
144d
Cleared
Oct 15, 1996
NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED
Orthopedic
56d
Cleared
Oct 01, 1996
INTERMOORE FRACTURE HIP STEM (MODIFY)
Orthopedic
57d
Cleared
Sep 03, 1996
SELECT SHOULDER COCR HUMERAL STEM COMPONENT
Orthopedic
78d
Cleared
Aug 29, 1996
SELECT SHOULDER COCR HUMERAL STEM COMPONENT
Orthopedic
76d
Cleared
Aug 28, 1996
SELECT SHOULDER CONCENTRIC HUMERAL HEAD COMPONENTS
Orthopedic
79d
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