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MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K081428
510(k) Type
Special
Applicant
BIOCOMPOSITES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/20/2008
Days to Decision
30 days
Submission Type
Summary

MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K081428
510(k) Type
Special
Applicant
BIOCOMPOSITES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/20/2008
Days to Decision
30 days
Submission Type
Summary