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Proficient™ Posterior Cervical Spine System

Page Type
Cleared 510(K)
510(k) Number
K162639
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2017
Days to Decision
138 days
Submission Type
Summary

Proficient™ Posterior Cervical Spine System

Page Type
Cleared 510(K)
510(k) Number
K162639
510(k) Type
Traditional
Applicant
Spine Wave, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2017
Days to Decision
138 days
Submission Type
Summary