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SMITH & NEPHEW PATIENT MATCHED CUTTING BLOCKS

K130708 Class II Traditional
Decision Date
2013-12-11
Sponsor / Applicant
Smith & Nephew, Inc.

Technical Specification

510(k) Submission ID K130708
Product Code JWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2013-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMITH & NEPHEW PATIENT MATCHED CUTTING BLOCKS received FDA 510(k) clearance under submission number K130708, sponsored by Smith & Nephew, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code JWH and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.