meddevicedb.com FDA Device Reference

SMR Stemless Anatomic

K221758 Class II Traditional
Decision Date
2023-03-17
Sponsor / Applicant
Lima Corporate S.P.A.

Technical Specification

510(k) Submission ID K221758
Product Code PKC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3660
Decision Date 2023-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMR Stemless Anatomic received FDA 510(k) clearance under submission number K221758, sponsored by Lima Corporate S.P.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code PKC and 21 CFR 888.3660, within the Orthopedic review panel as a Class II device.