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KESTREL POSTERIOR CERVICAL SPINE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132122
510(k) Type
Traditional
Applicant
OMNI SURGICAL LLC DBA SPINE360
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2014
Days to Decision
196 days
Submission Type
Summary

KESTREL POSTERIOR CERVICAL SPINE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132122
510(k) Type
Traditional
Applicant
OMNI SURGICAL LLC DBA SPINE360
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2014
Days to Decision
196 days
Submission Type
Summary