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Anatomic PEEK™ Cervical Fusion System with Nanotechnology

K230936 Class II Traditional
Decision Date
2023-06-02
Sponsor / Applicant
Nanovis, LLC

Technical Specification

510(k) Submission ID K230936
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2023-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Anatomic PEEK™ Cervical Fusion System with Nanotechnology received FDA 510(k) clearance under submission number K230936, sponsored by Nanovis, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code ODP and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.