meddevicedb.com FDA Device Reference

Restoration Anatomic Shell

K210893 Class II Special
Decision Date
2021-04-22
Sponsor / Applicant
Howmedica Osteonics Corp. A.K.A. Stryker Orthopaedics

Technical Specification

510(k) Submission ID K210893
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2021-04-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Restoration Anatomic Shell received FDA 510(k) clearance under submission number K210893, sponsored by Howmedica Osteonics Corp. A.K.A. Stryker Orthopaedics. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2021-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.