Clearance Summary
G Surgical Marksman Spinal Deformity System received FDA 510(k) clearance under submission number K230063, sponsored by G Surgical, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-02-09.
- Submission: K230063
- Applicant / Sponsor: G Surgical, LLC
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2023-02-09
Classification & Regulation
This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.