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RIVETTI-LEVINSON INSTRALUMINAL SHUNT

Page Type
Cleared 510(K)
510(k) Number
K972261
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1997
Days to Decision
90 days
Submission Type
Statement

RIVETTI-LEVINSON INSTRALUMINAL SHUNT

Page Type
Cleared 510(K)
510(k) Number
K972261
510(k) Type
Traditional
Applicant
INTEGRA NEUROCARE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1997
Days to Decision
90 days
Submission Type
Statement