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SEGMENTAL DEFECT REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980609
510(k) Type
Traditional
Applicant
METAGEN, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1998
Days to Decision
90 days
Submission Type
Summary

SEGMENTAL DEFECT REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980609
510(k) Type
Traditional
Applicant
METAGEN, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1998
Days to Decision
90 days
Submission Type
Summary