Last synced on 14 November 2025 at 11:06 pm

WEREWOLF COBLATION System, COBLATION HALO Wand

Page Type
Cleared 510(K)
510(k) Number
K192027
510(k) Type
Traditional
Applicant
Arthrocare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
144 days
Submission Type
Summary

WEREWOLF COBLATION System, COBLATION HALO Wand

Page Type
Cleared 510(K)
510(k) Number
K192027
510(k) Type
Traditional
Applicant
Arthrocare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2019
Days to Decision
144 days
Submission Type
Summary