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CORDIS HI-FLEX PERVENOUS ACTIVE FIXATION UNIPOLAR

Page Type
Cleared 510(K)
510(k) Number
K851064
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1986
Days to Decision
508 days

CORDIS HI-FLEX PERVENOUS ACTIVE FIXATION UNIPOLAR

Page Type
Cleared 510(K)
510(k) Number
K851064
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1986
Days to Decision
508 days