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BIOLOK SCREW, BIOSTEON SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003641
510(k) Type
Traditional
Applicant
BIOCOMPOSITES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/8/2001
Days to Decision
73 days
Submission Type
Summary

BIOLOK SCREW, BIOSTEON SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003641
510(k) Type
Traditional
Applicant
BIOCOMPOSITES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/8/2001
Days to Decision
73 days
Submission Type
Summary