Mako Surgical Corporation is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mako Surgical Corporation - FDA 510(k) Cleared Devices
Recent clearances: Partial Knee Application (PKA), RESTORIS POROUS PARTIAL KNEE SYSTEM, MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM
8
Total
8
Cleared
0
Denied
Mako Surgical Corporation has 8 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.
Historical record: 8 cleared submissions from 2008 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Mako Surgical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mako Surgical Corporation
8 devices
Cleared
Sep 16, 2015
Partial Knee Application (PKA)
Orthopedic
372d
Cleared
Mar 20, 2015
RESTORIS POROUS PARTIAL KNEE SYSTEM
Orthopedic
30d
Cleared
Nov 13, 2014
MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM
Orthopedic
114d
Cleared
Dec 10, 2013
RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM
Orthopedic
75d
Cleared
Jun 06, 2012
MAKOPLASTY TOTAL HIP APPLICATION, RIO STANDARD SYSTEM
Orthopedic
61d
Cleared
Mar 01, 2012
RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM
Orthopedic
184d
Cleared
Jun 17, 2009
RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM
Orthopedic
86d
Cleared
Nov 28, 2008
MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM
Orthopedic
119d