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PECTOFIX STERNAL REPAIR WIRE

Page Type
Cleared 510(K)
510(k) Number
K003951
510(k) Type
Traditional
Applicant
PECTOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2001
Days to Decision
90 days
Submission Type
Summary

PECTOFIX STERNAL REPAIR WIRE

Page Type
Cleared 510(K)
510(k) Number
K003951
510(k) Type
Traditional
Applicant
PECTOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2001
Days to Decision
90 days
Submission Type
Summary