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Standard Staple-Line Reinforcement (SSLR23)

K231603 Class II Traditional
Decision Date
2023-10-06
Sponsor / Applicant
Standard Bariatrics, Inc.

Technical Specification

510(k) Submission ID K231603
Product Code OXC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2023-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Standard Staple-Line Reinforcement (SSLR23) received FDA 510(k) clearance under submission number K231603, sponsored by Standard Bariatrics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2023-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code OXC and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.