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Reprocessed ArthroCare ENT Coblator

Page Type
Cleared 510(K)
510(k) Number
K172647
510(k) Type
Traditional
Applicant
ReNovo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2018
Days to Decision
173 days
Submission Type
Summary

Reprocessed ArthroCare ENT Coblator

Page Type
Cleared 510(K)
510(k) Number
K172647
510(k) Type
Traditional
Applicant
ReNovo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2018
Days to Decision
173 days
Submission Type
Summary