Last synced on 18 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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