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Orbit Subretinal Delivery System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182274
510(k) Type
Traditional
Applicant
Orbit Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
11/20/2018
Days to Decision
90 days
Submission Type
Summary

Orbit Subretinal Delivery System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182274
510(k) Type
Traditional
Applicant
Orbit Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
11/20/2018
Days to Decision
90 days
Submission Type
Summary