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ISA-21 INTERVENTIONAL SPINE ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K021631
510(k) Type
Traditional
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2002
Days to Decision
88 days
Submission Type
Statement

ISA-21 INTERVENTIONAL SPINE ARRAY COIL

Page Type
Cleared 510(K)
510(k) Number
K021631
510(k) Type
Traditional
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2002
Days to Decision
88 days
Submission Type
Statement