TECHFIT DISRP® System— 510(k) K230276

Substantially Equivalent

Techfit Digital Surgery

FDA 510(k) clearance K230276 for TECHFIT DISRP® System, Substantially Equivalent on 2023-06-23. Applicant: Techfit Digital Surgery. Device class: 2.

Clearance details

Applicant: Techfit Digital Surgery
Product code: Code DZJ
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2023-02-01
Decision date: 2023-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Daytona Beach, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZJ

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K223024 — MedCAD AccuPlan System2023-03-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.