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OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112214
510(k) Type
Traditional
Applicant
ST. JUDE MEDICAL NEUROMODULATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2011
Days to Decision
107 days
Submission Type
Statement

OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112214
510(k) Type
Traditional
Applicant
ST. JUDE MEDICAL NEUROMODULATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2011
Days to Decision
107 days
Submission Type
Statement