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Reprocessed ArthoCare Ablation Wand

Page Type
Cleared 510(K)
510(k) Number
K173741
510(k) Type
Traditional
Applicant
ReNovo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2018
Days to Decision
88 days
Submission Type
Summary

Reprocessed ArthoCare Ablation Wand

Page Type
Cleared 510(K)
510(k) Number
K173741
510(k) Type
Traditional
Applicant
ReNovo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2018
Days to Decision
88 days
Submission Type
Summary