Medical Device Manufacturer · US , Fort Lauderdale , FL

Mako Surgical Corporation - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2008
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
1-8 of 8
Cleared Sep 16, 2015
Partial Knee Application (PKA)
K142530 · OLO
Orthopedic · 372d
Cleared Mar 20, 2015
RESTORIS POROUS PARTIAL KNEE SYSTEM
K150410 · HRY
Orthopedic · 30d
Cleared Nov 13, 2014
MAKOPLASTY TOTAL HIP ALLPICATION, RIO STANDARD SYSTEM
K141989 · OLO
Orthopedic · 114d
Cleared Dec 10, 2013
RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM
K133039 · NPJ
Orthopedic · 75d
Cleared Jun 06, 2012
MAKOPLASTY TOTAL HIP APPLICATION, RIO STANDARD SYSTEM
K121064 · OLO
Orthopedic · 61d
Cleared Mar 01, 2012
RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM
K112507 · OLO
Orthopedic · 184d
Cleared Jun 17, 2009
RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM
K090763 · NPJ
Orthopedic · 86d
Cleared Nov 28, 2008
MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM
K082172 · HSX
Orthopedic · 119d
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