Sulzer Spine-Tech is one of 11992 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sulzer Spine-Tech - FDA 510(k) Cleared Devices
Recent clearances: SILHOUETTE SPINAL FIXATION SYSTEM, MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM
7
Total
7
Cleared
0
Denied
Sulzer Spine-Tech has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 7 cleared submissions from 1999 to 2002. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sulzer Spine-Tech Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sulzer Spine-Tech
7 devices
Cleared
Sep 24, 2002
CADENCE SPINAL FIXATION SYSTEM
Orthopedic
64d
Cleared
May 02, 2002
RPX TITANIUM CEMNT RESTRICTOR
Orthopedic
90d
Cleared
Feb 15, 2002
MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM
Orthopedic
24d
Cleared
Sep 28, 2001
DEVICE MODIFICATION OF SILHOUETTE SPINDAL FIXATION SYSTEM
Orthopedic
78d
Cleared
Aug 22, 2001
MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
30d
Cleared
Nov 16, 1999
SILHOUETTE SPINAL FIXATION SYSTEM
Orthopedic
64d
Cleared
Oct 01, 1999
MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM
Orthopedic
86d