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RENEW NEUROSTIMULATION SYSTEM

Page Type
Cleared 510(K)
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)
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