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ORTHOALIGN PLUS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130387
510(k) Type
Traditional
Applicant
ORTHALIGN, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2013
Days to Decision
266 days
Submission Type
Summary

ORTHOALIGN PLUS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130387
510(k) Type
Traditional
Applicant
ORTHALIGN, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2013
Days to Decision
266 days
Submission Type
Summary