Precision Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Spine - FDA 510(k) Cleared Devices
Recent clearances: Reform Pedicle Screw System, NexGen Anterior Cervical Plate System
2
Total
2
Cleared
0
Denied
Precision Spine has 2 FDA 510(k) cleared medical devices. Based in Pear, US.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Precision Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Precision Spine
2 devices