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KESTREL POSTERIOR CERVICAL SPINE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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