GXL — Screwdriver, Skullplate Class I
FDA product code GXL covers "Screwdriver, Skullplate", a Class I medical device regulated under 21 CFR 882.4900. Submissions are reviewed by the Neurology panel.
Classification Details
- Product Code
- GXL
- Device Class
- Class I
- Regulation Number
- 882.4900
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No