Last synced on 14 November 2025 at 11:06 pm

ARTHREX IBALANCE TKA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K141635
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2014
Days to Decision
76 days
Submission Type
Summary

ARTHREX IBALANCE TKA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K141635
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2014
Days to Decision
76 days
Submission Type
Summary