Medical Device Manufacturer · US , Ashland , MA

Renovis Surgical Technologies, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2014
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Renovis Surgical Technologies, Inc. Orthopedic ✕
7 devices
1-7 of 7
Cleared Jun 14, 2018
S128 Anterior Lumbar Interbody Fusion (ALIF) System
K180502 · OVD
Orthopedic · 108d
Cleared Sep 25, 2015
Renovis Anterior Cervical Plate System
K152193 · KWQ
Orthopedic · 51d
Cleared May 11, 2015
Renovis Surgical Hip Replacement System
K143647 · OQG
Orthopedic · 140d
Cleared Nov 04, 2014
RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM
K141676 · LPH
Orthopedic · 134d
Cleared Oct 15, 2014
RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
K142095 · OVD
Orthopedic · 75d
Cleared Sep 02, 2014
RENOVIS CEMENTED HIP SYSTEM
K141370 · JDI
Orthopedic · 98d
Cleared Mar 27, 2014
S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
K140106 · OVD
Orthopedic · 71d
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