Orthomet, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthomet, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ORTHOMET HMC FEMORAL STEM COMPONENT, ORTHOMET TITANIUM HYBRID FEMORAL STEM, ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY
60
Total
41
Cleared
0
Denied
Orthomet, Inc. has 41 FDA 510(k) cleared orthopedic devices. Based in Plymouth, US.
Historical record: 41 cleared submissions from 1986 to 1995.
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 - Orthomet, Inc.
60 devices
Cleared
Jun 07, 1995
ORTHOMET HMC FEMORAL STEM COMPONENT
Orthopedic
426d
Cleared
May 30, 1995
ORTHOMET TITANIUM HYBRID FEMORAL STEM
Orthopedic
186d
Cleared
Apr 26, 1995
ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY
Orthopedic
260d
Cleared
Dec 28, 1994
ORTHOMET RESURFACING FEMORAL COMPONENT
Orthopedic
93d
Cleared
Nov 30, 1994
PERFECTA TOTAL HIP SYSTEM COATED COCR FEMORAL STEM
Orthopedic
652d
Cleared
Oct 18, 1994
AXIOM TOTAL KNEE SYST/ACL RETAIN TIBIAL TRAY/INSER
Orthopedic
671d
Cleared
Oct 14, 1994
ORTHOMET ACETABULAR CUP SYSTEM
Orthopedic
577d
Cleared
Oct 14, 1994
ORTHOMET LHMC FEMORAL STEM
Ophthalmic
556d
Cleared
Oct 14, 1994
AXIOM TOTAL KNEE SYSTEM
Orthopedic
499d
Cleared
Jan 07, 1994
PERFECTA TOTAL HIP SYSTEM
Orthopedic
554d
Cleared
Jan 07, 1994
HYBRID FEMORAL STEM, PERFECTA TOTAL HIP SYSTEM
Orthopedic
431d
Cleared
Oct 27, 1993
AXIOM TOTAL KNEE SYSTEM, MODULAR TIBIAL TRAY
Orthopedic
405d
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