Last synced on 14 November 2025 at 11:06 pm

KNEEALIGN SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K091411
510(k) Type
Traditional
Applicant
ORTHALIGN, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2009
Days to Decision
135 days
Submission Type
Summary

KNEEALIGN SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K091411
510(k) Type
Traditional
Applicant
ORTHALIGN, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2009
Days to Decision
135 days
Submission Type
Summary