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NuVasive Specialized Orthopedics, Inc.

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 26 recall (Z-0500-2025)NuVasive Specialized Orthopedics, Inc.2024-11-21
NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to m recall (Z-0559-2023)NuVasive Specialized Orthopedics, Inc.2022-12-14
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/I recall (Z-0319-2022)NuVasive Specialized Orthopedics, Inc.2021-12-01
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System End Cap for PRE recall (Z-1349-2021)Nuvasive Specialized Orthopedics Inc2021-04-05
NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail System/PRECICE Unyt recall (Z-1350-2021)Nuvasive Specialized Orthopedics Inc2021-04-05
NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Pack recall (Z-1351-2021)Nuvasive Specialized Orthopedics Inc2021-04-05
PRECICE STRYDE - Product Usage: intended for limb lengthening, open and closed fracture fi recall (Z-1323-2021)Nuvasive Specialized Orthopedics Inc2021-03-30
Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fra recall (Z-1324-2021)Nuvasive Specialized Orthopedics Inc2021-03-30
PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fix recall (Z-1325-2021)Nuvasive Specialized Orthopedics Inc2021-03-30

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Every clearance here is in the API, with alerts when new ones post.