Depuy Spine, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Spine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CONFIDENCE Spinal Cement System, EXPEDIUM VERSE SPINE SYSTEM, EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
68
Total
67
Cleared
0
Denied
Depuy Spine, Inc. has 67 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.
Historical record: 67 cleared submissions from 2004 to 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Depuy Spine, Inc.
68 devices
Cleared
Aug 31, 2020
CONFIDENCE Spinal Cement System
Orthopedic
60d
Cleared
Nov 19, 2014
EXPEDIUM VERSE SPINE SYSTEM
Orthopedic
103d
Cleared
Jun 14, 2012
EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
Orthopedic
419d
Cleared
May 03, 2012
VIPER SYSTEM
Orthopedic
29d
Cleared
Apr 07, 2011
MOUNTAINEER OCT SPINAL SYSTEM
Orthopedic
59d
Cleared
Apr 01, 2011
EXPEDIUM SYSTEM, VIPER SYSTEM
Orthopedic
66d
Cleared
Jan 18, 2011
VEPER SYSTEM, EXPEDIUM SYSTEM
Orthopedic
85d
Cleared
Dec 07, 2010
VIPER SYSTEM, EXPEDIUM SYSTEM
Orthopedic
145d
Cleared
Nov 17, 2010
MOUNTAINEER OCT SPINAL SYSTEM
Orthopedic
28d
Cleared
Nov 15, 2010
VIPER F2 FACET FIXATION SYSTEM
Orthopedic
146d
Cleared
Oct 20, 2010
VIPER SPINE SYSTEM
Orthopedic
30d
Cleared
Oct 18, 2010
MODIFICATION TO:EXPEDIUM SPINE SYSTEM
Orthopedic
98d
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