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Ekso™ (version 1.1) and Ekso GT™ (version 1.2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161443
510(k) Type
Traditional
Applicant
EKSO BIONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2016
Days to Decision
55 days
Submission Type
Summary

Ekso™ (version 1.1) and Ekso GT™ (version 1.2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161443
510(k) Type
Traditional
Applicant
EKSO BIONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2016
Days to Decision
55 days
Submission Type
Summary