Howmedica, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Howmedica, Inc. - FDA 510(k) Cleared Devices
Recent clearances: XIA SPINE SYSTEM, HOWMEDICA HUMERAL INTERCALARY SYSTEM, ZETA MULTIZONE LOCKING NAIL SYSTEM
36
Total
29
Cleared
0
Denied
Howmedica, Inc. has 29 FDA 510(k) cleared orthopedic devices. Based in Rutherford, US.
Historical record: 29 cleared submissions from 1994 to 1999.
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 - Howmedica, Inc.
36 devices
Cleared
Feb 24, 1999
XIA SPINE SYSTEM
Orthopedic
89d
Cleared
Feb 05, 1999
HOWMEDICA HUMERAL INTERCALARY SYSTEM
Orthopedic
73d
Cleared
Feb 01, 1999
ZETA MULTIZONE LOCKING NAIL SYSTEM
Orthopedic
61d
Cleared
Jan 29, 1999
BURR HOLE COVERS, CRANIOMAXILLOFACIAL PLATES
Dental
88d
Cleared
Nov 18, 1998
G/K SFN AND STN LOCKING NAILS
Orthopedic
55d
Cleared
Sep 30, 1998
EXTRACRANIAL RADIOTHERAPY SYSTEM
Radiology
77d
Cleared
Aug 31, 1998
HOWMEDICA ASYMMETRIC STEM VITALOCK CLUSTER & SPIKED SHELLS, AND ACETABULAR...
Orthopedic
66d
Cleared
Jun 26, 1998
RELIANCE LONG STEM FEMORAL COMPONENTS
Orthopedic
115d
Cleared
Jun 10, 1998
ROGACHEFSKY DISTAL RADIUS PLATES
Orthopedic
63d
Cleared
Jun 02, 1998
EXETER INTRAMEDULLARY BONE PLUG
Orthopedic
90d
Cleared
Apr 16, 1998
PARTNERSHIP CALCAR FEMORAL COMPONENTS
Orthopedic
83d
Cleared
Mar 13, 1998
HOWMEDICA(R) FULLY THREADED SCREWS
Orthopedic
85d