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DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061166
510(k) Type
Traditional
Applicant
BIOWAVE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2006
Days to Decision
110 days
Submission Type
Summary

DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061166
510(k) Type
Traditional
Applicant
BIOWAVE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2006
Days to Decision
110 days
Submission Type
Summary