FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

G Surgical Marksman Spinal Deformity System

K Number: K230063 · Decision Feb 9, 2023
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
7
Review Days
31

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Basic Information

Device Name
G Surgical Marksman Spinal Deformity System
K Number
K230063
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
G Surgical, LLC
Date Received
January 9, 2023
Decision Date
February 9, 2023
Product Code
NKB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NKB Thoracolumbosacral Pedicle Screw System

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K Number Device Name
K240737 G Surgical Marksman MIS System
K210890 GPS Cervical Spacers
K193219 G Surgical Marksman System
K171834 G Surgical OCT Spinal System
K161516 G Surgical Marksman MIS System
K142456 GPS Spacers