Medicrea International SA - FDA 510(k) Cleared Devices
25
Total
25
Cleared
0
Denied
Medicrea International SA has 25 FDA 510(k) cleared orthopedic devices. Based in Neyron, FR.
Last cleared in 2022. Active since 2015.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medicrea International SA
25 devices
Cleared
May 24, 2022
LigaPASS™ 2.0 Ligament Augmentation System
Orthopedic
186d
Cleared
Jan 05, 2022
PASS LP™ Spinal System, CD Horizon™ Spinal System
Orthopedic
96d
Cleared
Sep 03, 2021
C-CURVE Interbody Fusion Device
Orthopedic
198d
Cleared
Oct 30, 2020
UNiD IB3D ALIF
Orthopedic
266d
Cleared
Oct 30, 2019
IB3D ALIF
Orthopedic
184d
Cleared
Jul 15, 2019
UNiD Patient-matched PLIF cage
Orthopedic
340d
Cleared
May 08, 2019
UNiD Patient specific 3D printed TLIF cage
Orthopedic
110d
Cleared
May 02, 2019
PASS LP Spinal System
Orthopedic
72d
Cleared
Oct 17, 2018
PASS LP Spinal System
Orthopedic
58d
Cleared
Apr 25, 2018
UNiD Patient Specific 3D printed cage
Orthopedic
133d
Cleared
Apr 03, 2018
LigaPASS
Orthopedic
141d
Cleared
Nov 13, 2017
IMPIX 3D Print Cages
Orthopedic
327d