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Sequel External Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K202833
510(k) Type
Traditional
Applicant
Sequel Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2021
Days to Decision
116 days
Submission Type
Summary

Sequel External Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K202833
510(k) Type
Traditional
Applicant
Sequel Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2021
Days to Decision
116 days
Submission Type
Summary