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ZIMMER MOTIONLOC SCREW FOR PERIARTICULAR LOCKING PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130810
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2013
Days to Decision
178 days
Submission Type
Summary

ZIMMER MOTIONLOC SCREW FOR PERIARTICULAR LOCKING PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130810
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2013
Days to Decision
178 days
Submission Type
Summary