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BIOCUFF, MODELS 225718, 225728, 225736, 235718, 235728, 235736

Page Type
Cleared 510(K)
510(k) Number
K001378
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/28/2000
Days to Decision
88 days
Submission Type
Summary

BIOCUFF, MODELS 225718, 225728, 225736, 235718, 235728, 235736

Page Type
Cleared 510(K)
510(k) Number
K001378
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, INC.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/28/2000
Days to Decision
88 days
Submission Type
Summary