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DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE

Page Type
Cleared 510(K)
510(k) Number
K013513
510(k) Type
Traditional
Applicant
PAIN CONCEPTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2002
Days to Decision
87 days
Submission Type
Statement

DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE

Page Type
Cleared 510(K)
510(k) Number
K013513
510(k) Type
Traditional
Applicant
PAIN CONCEPTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2002
Days to Decision
87 days
Submission Type
Statement