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SUPER REVO SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K003984
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2001
Days to Decision
83 days
Submission Type
Summary

SUPER REVO SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K003984
510(k) Type
Traditional
Applicant
LINVATEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2001
Days to Decision
83 days
Submission Type
Summary