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GEMINUS FOSSA SPECIFIC PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122310
510(k) Type
Traditional
Applicant
SKELETAL DYNAMICS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2013
Days to Decision
170 days
Submission Type
Summary

GEMINUS FOSSA SPECIFIC PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122310
510(k) Type
Traditional
Applicant
SKELETAL DYNAMICS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2013
Days to Decision
170 days
Submission Type
Summary