Nuvasive Specialized Orthopedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nuvasive Specialized Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Precice Ankle Salvage System, Precice Intramedullary Limb Lengthening System, External Remote Controller ERC 4P
20
Total
20
Cleared
0
Denied
Nuvasive Specialized Orthopedics, Inc. has 20 FDA 510(k) cleared orthopedic devices. Based in Alisa Viejo, US.
Last cleared in 2023. Active since 2016.
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 - Nuvasive Specialized Orthopedics, Inc.
20 devices
Cleared
Aug 29, 2023
Precice Ankle Salvage System
Orthopedic
162d
Cleared
Mar 15, 2023
Precice Intramedullary Limb Lengthening System
Orthopedic
412d
Cleared
Dec 22, 2020
External Remote Controller ERC 4P
Orthopedic
126d
Cleared
Sep 16, 2020
Precice® Ankle Salvage System
Orthopedic
208d
Cleared
Aug 10, 2020
Precice® Bone Transport System
Orthopedic
60d
Cleared
Jul 30, 2020
MAGEC® System
Orthopedic
51d
Cleared
May 08, 2020
PRECICE Bone Transport System
Orthopedic
192d
Cleared
May 08, 2020
Precice® Screws
Orthopedic
134d
Cleared
Nov 07, 2019
PRECICE Plating System
Orthopedic
87d
Cleared
Sep 26, 2019
PRECICE System
Orthopedic
132d
Cleared
Feb 05, 2019
PRECICE® BONE TRANSPORT™ System
Orthopedic
179d
Cleared
Apr 03, 2018
PRECICE STRYDE System
Orthopedic
36d