Nextremity Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nextremity Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Nextra CH Cannulated Hammertoe System, CalcShift™ Displacement Calcaneal Osteotomy System, StealthFix Intraosseous Fixation System
17
Total
17
Cleared
0
Denied
Nextremity Solutions, Inc. has 17 FDA 510(k) cleared orthopedic devices. Based in Red Bank, US.
Last cleared in 2022. 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.
FDA 510(k) Regulatory Record - Nextremity Solutions, Inc.
17 devices
Cleared
Nov 04, 2022
Nextra CH Cannulated Hammertoe System
Orthopedic
154d
Cleared
May 20, 2022
CalcShift™ Displacement Calcaneal Osteotomy System
Orthopedic
245d
Cleared
Mar 22, 2022
StealthFix Intraosseous Fixation System
Orthopedic
60d
Cleared
Dec 21, 2021
InCore Subtalar System
Orthopedic
81d
Cleared
Dec 09, 2021
Nextra CH Cannulated Hammertoe System
Orthopedic
34d
Cleared
Nov 18, 2021
Stratum® Ankle Fusion Plating System
General Hospital
90d
Cleared
Sep 23, 2021
Nexta PEEK Hammertoe Correction System
Orthopedic
87d
Cleared
Jul 27, 2020
Stratum™ Reduced Size Foot Plating System
Orthopedic
123d
Cleared
Jun 26, 2020
DuoHex CH Cannulated Hammertoe System
Orthopedic
87d
Cleared
May 13, 2020
InCore MPJ System
Orthopedic
113d
Cleared
Dec 31, 2019
InCore TMT System
Orthopedic
103d
Cleared
May 24, 2019
InCore® Lapidus Sterile Kits
Orthopedic
107d