Last synced on 14 November 2025 at 11:06 pm

ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND

Page Type
Cleared 510(K)
510(k) Number
K132099
510(k) Type
Traditional
Applicant
ARTHROCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2013
Days to Decision
45 days
Submission Type
Summary

ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND

Page Type
Cleared 510(K)
510(k) Number
K132099
510(k) Type
Traditional
Applicant
ARTHROCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2013
Days to Decision
45 days
Submission Type
Summary