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# Orthopedic/Rehabilitation Devices Panel Meeting 9/8-9
- URL: https://www.fdaweb.com/orthopedic-rehabilitation-devices-panel-meeting-9-8-9/
- Published: 2020-07-29T12:00:00.000Z
- Updated: 2026-09-14T16:22:57.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5147308

*Federal Register* notice: FDA is announcing a 9/8-9 virtual meeting of its Orthopedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee. On 9/8, panel members are scheduled to discuss and make recommendations on the classification of facet screws systems, which are currently unclassified pre-amendment devices, to Class 2 (general and special controls). They will also discuss and make recommendations on the reclassification of non-invasive bone growth stimulators from Class 3 (general controls and premarket approval) to Class 2 (general and special controls). On 9/9, the committee will discuss and make recommendations regarding the classification of three devices, which are currently unclassified pre-amendment devices to Class 2 (general and special controls) —semi-constrained toe (metatarsophalangeal) joint prostheses, intracompartmental pressure monitors, and intra-abdominal pressure monitoring devices. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-07-29/pdf/2020-16436.pdf?ref=fdaweb.com).