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NUCLEOTOMY INTRADISCAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K013622
510(k) Type
Traditional
Applicant
ORATEC INTERVENTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2002
Days to Decision
87 days
Submission Type
Summary

NUCLEOTOMY INTRADISCAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K013622
510(k) Type
Traditional
Applicant
ORATEC INTERVENTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2002
Days to Decision
87 days
Submission Type
Summary