Last synced on 17 January 2025 at 11:05 pm

ARIS¿ COBLATION¿ Turbinate Reduction Wand (72290113); WEREWOLF COBLATION System (72290144); WEREWOLF+ COBLATION System (72290146)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230914
510(k) Type
Traditional
Applicant
Arthrocare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2023
Days to Decision
87 days
Submission Type
Summary