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PERIARTICULAR LOCKING PLATES AND SCREWS, MODEL 2358 SERIES

Page Type
Cleared 510(K)
510(k) Number
K051098
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2005
Days to Decision
69 days
Submission Type
Summary

PERIARTICULAR LOCKING PLATES AND SCREWS, MODEL 2358 SERIES

Page Type
Cleared 510(K)
510(k) Number
K051098
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2005
Days to Decision
69 days
Submission Type
Summary