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Boomerang™ Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K190227
510(k) Type
Traditional
Applicant
ChoiceSpine, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2019
Days to Decision
85 days
Submission Type
Summary

Boomerang™ Anterior Cervical Plate System

Page Type
Cleared 510(K)
510(k) Number
K190227
510(k) Type
Traditional
Applicant
ChoiceSpine, LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2019
Days to Decision
85 days
Submission Type
Summary