Last synced on 14 November 2025 at 11:06 pm

ORISE ProKnife

Page Type
Cleared 510(K)
510(k) Number
K200404
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2020
Days to Decision
288 days
Submission Type
Summary

ORISE ProKnife

Page Type
Cleared 510(K)
510(k) Number
K200404
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2020
Days to Decision
288 days
Submission Type
Summary