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# Device Panel to Review 5 Classifications
- URL: https://www.fdaweb.com/device-panel-to-review-5-classifications/
- Published: 2020-02-21T12:00:00.000Z
- Updated: 2026-09-14T16:04:01.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146146

*Federal Register* notice: FDA has announced a 4/23-24 Orthopedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee meeting. On 4/23, panel members will discuss the classification of facet screws systems, which are currently unclassified pre-amendment devices, to Class 2 (general and special controls). They will also discuss the reclassification of noninvasive bone growth stimulators from Class 3 to Class 2\. On 4/24, the panel will discuss the classification of three devices, which are currently unclassified pre-amendment devices to Class 2\. The devices under discussion are semi-constrained toe joint prostheses; intra-compartmental pressure monitors, intra-abdominal pressure monitors. To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2020-03565.pdf?ref=fdaweb.com).