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DOUBLEPLAY SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061949
510(k) Type
Traditional
Applicant
BIOCOMPOSITES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/25/2006
Days to Decision
77 days
Submission Type
Summary

DOUBLEPLAY SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061949
510(k) Type
Traditional
Applicant
BIOCOMPOSITES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/25/2006
Days to Decision
77 days
Submission Type
Summary