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MULTISTIM LAMINECTOMY ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K853643
510(k) Type
Traditional
Applicant
NEUROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1985
Days to Decision
72 days

MULTISTIM LAMINECTOMY ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K853643
510(k) Type
Traditional
Applicant
NEUROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1985
Days to Decision
72 days