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PERIARTICULAR LOCKING PLATES AND SCREWS, 2358, 2359 SERIES

Page Type
Cleared 510(K)
510(k) Number
K040593
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2004
Days to Decision
35 days
Submission Type
Summary

PERIARTICULAR LOCKING PLATES AND SCREWS, 2358, 2359 SERIES

Page Type
Cleared 510(K)
510(k) Number
K040593
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2004
Days to Decision
35 days
Submission Type
Summary