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510(k) clearance

Kentrospine Viktr-MIS® Pedicle screw system

FDA 510(k) source

510(k) number
K252139
Applicant
Rivarp Medical Pvt., Ltd.
Decision date
Sep 27, 2026
Date received
Jul 8, 2025
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
NKB
Device type
Thoracolumbosacral Pedicle Screw System
Device class
Class II
Regulation
21 CFR 888.3070
Advisory committee
Orthopedic
Statement or summary
Summary
Third party
N
Location
Bangalore, IN