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Orbit Subretinal Delivery System

Page Type
Cleared 510(K)
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)
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