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KNEEALIGN SYSTEM WITH REFERENCE SENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093998
510(k) Type
Special
Applicant
ORTHALIGN, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2010
Days to Decision
84 days
Submission Type
Summary

KNEEALIGN SYSTEM WITH REFERENCE SENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093998
510(k) Type
Special
Applicant
ORTHALIGN, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2010
Days to Decision
84 days
Submission Type
Summary