Last synced on 14 November 2025 at 11:06 pm

Arcos One-piece Femoral Revision System

Page Type
Cleared 510(K)
510(k) Number
K151603
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2015
Days to Decision
116 days
Submission Type
Summary

Arcos One-piece Femoral Revision System

Page Type
Cleared 510(K)
510(k) Number
K151603
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2015
Days to Decision
116 days
Submission Type
Summary