Last synced on 14 November 2025 at 11:06 pm

COMPREHENSIVE REVERSE SHOULDER

Page Type
Cleared 510(K)
510(k) Number
K080642
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2008
Days to Decision
125 days
Submission Type
Summary

COMPREHENSIVE REVERSE SHOULDER

Page Type
Cleared 510(K)
510(k) Number
K080642
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2008
Days to Decision
125 days
Submission Type
Summary