Surgtech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SurgTech GENOLL Total Knee System, SurgTech Bipolar Head System
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgtech, Inc. Orthopedic ✕
6 devices
Cleared
Aug 01, 2019
SurgTech GENOLL Total Knee System
Orthopedic
90d
Cleared
Jun 14, 2018
SurgTech Bipolar Head System
Orthopedic
219d
Cleared
May 10, 2017
MALUC™ Total Hip Arthroplasty System
Orthopedic
282d
Cleared
Apr 05, 2017
SurgTech Thoracolumbosacral (TLS) Posterior Fixation System
Orthopedic
126d
Cleared
Feb 21, 2017
SurgTech Trauma System
Orthopedic
225d
Cleared
Mar 25, 2016
SurgTech Interbody System
Orthopedic
232d