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LUMBAR DRAINAGE ACCESSORY KIT

Page Type
Cleared 510(K)
510(k) Number
K970658
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1997
Days to Decision
87 days
Submission Type
Statement

LUMBAR DRAINAGE ACCESSORY KIT

Page Type
Cleared 510(K)
510(k) Number
K970658
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1997
Days to Decision
87 days
Submission Type
Statement