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ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM, MODEL 2357 & 2359

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050121
510(k) Type
Special
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2005
Days to Decision
12 days
Submission Type
Summary

ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM, MODEL 2357 & 2359

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050121
510(k) Type
Special
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2005
Days to Decision
12 days
Submission Type
Summary