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pNOVUS 21 Microcatheter

Page Type
Cleared 510(K)
510(k) Number
K221279
510(k) Type
Traditional
Applicant
phenox Ltd
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
11/28/2022
Days to Decision
209 days
Submission Type
Summary

pNOVUS 21 Microcatheter

Page Type
Cleared 510(K)
510(k) Number
K221279
510(k) Type
Traditional
Applicant
phenox Ltd
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
11/28/2022
Days to Decision
209 days
Submission Type
Summary