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AlignMATE™ Lapidus Arthrodesis System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162391
510(k) Type
Special
Applicant
ARTHROSURFACE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2017
Days to Decision
179 days
Submission Type
Summary

AlignMATE™ Lapidus Arthrodesis System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162391
510(k) Type
Special
Applicant
ARTHROSURFACE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2017
Days to Decision
179 days
Submission Type
Summary