In2bones Sas is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
In2bones Sas - FDA 510(k) Cleared Devices
Recent clearances: QUANTUM® Patient Specific Instrumentation (PSI) System, QUANTUM Patient Specific Instrumentation (PSI) System, QUANTUM® Patient Specific Instrumentation (PSI) System
18
Total
18
Cleared
0
Denied
In2bones Sas has 18 FDA 510(k) cleared orthopedic devices. Based in Potomac, US.
Latest FDA clearance: Apr 2024. Active since 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by In2bones USA and Mrc-X, LLC.
FDA 510(k) Regulatory Record - In2bones Sas
18 devices
Cleared
Apr 23, 2024
QUANTUM® Patient Specific Instrumentation (PSI) System
Orthopedic
316d
Cleared
Apr 06, 2023
QUANTUM Patient Specific Instrumentation (PSI) System
Orthopedic
59d
Cleared
Aug 11, 2021
QUANTUM® Patient Specific Instrumentation (PSI) System
Orthopedic
51d
Cleared
Jan 29, 2020
Quantum® Total Ankle Prosthesis
Orthopedic
251d
Cleared
Mar 15, 2018
TRIWAY Tibiotalocalcaneal (TTC) Arthrodesis System
Orthopedic
90d
Cleared
Jan 19, 2018
DIP Arthrodesis System
Orthopedic
58d
Cleared
Nov 28, 2017
PIT’Stop® implant
Orthopedic
266d
Cleared
Nov 28, 2017
Ankle Fusion Plating System
Orthopedic
60d
Cleared
May 10, 2017
I.B.S. osteosynthesis screws
Orthopedic
71d
Cleared
Oct 06, 2016
I.B.S. 2.0 Osteosynthesis screw
Orthopedic
253d
Cleared
Jun 10, 2016
NEOVIEW Plating System
Orthopedic
63d
Cleared
Mar 21, 2016
OS2(R)-VP Varisation Staple
Orthopedic
82d