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RENEW NEUROSTIMULATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000852
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2001
Days to Decision
310 days
Submission Type
Summary

RENEW NEUROSTIMULATION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000852
510(k) Type
Traditional
Applicant
ADVANCED NEUROMODULATION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2001
Days to Decision
310 days
Submission Type
Summary