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Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200); Turbett Surgical Instrument Pod (TS1000)

K250011 Class II Traditional
Decision Date
2025-04-04
Sponsor / Applicant
Turbett Surgical

Technical Specification

510(k) Submission ID K250011
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2025-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200); Turbett Surgical Instrument Pod (TS1000) received FDA 510(k) clearance under submission number K250011, sponsored by Turbett Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2025-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code FRG and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.