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SUPER REVO HERCULINE SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K041713
510(k) Type
Special
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2004
Days to Decision
29 days
Submission Type
Summary

SUPER REVO HERCULINE SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K041713
510(k) Type
Special
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2004
Days to Decision
29 days
Submission Type
Summary