meddevicedb.com FDA Device Reference

Pisces-SC Standalone Cervical Interbody System

K261882 Class II Traditional
Decision Date
2026-08-21
Sponsor / Applicant
Osseus Fusions Systems, LLC

Technical Specification

510(k) Submission ID K261882
Product Code OVE
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2026-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pisces-SC Standalone Cervical Interbody System received FDA 510(k) clearance under submission number K261882, sponsored by Osseus Fusions Systems, 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 2026-08-21.

Classification & Regulation

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