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VELOX ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131521
510(k) Type
Traditional
Applicant
SPINECRAFT LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2013
Days to Decision
210 days
Submission Type
Summary

VELOX ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131521
510(k) Type
Traditional
Applicant
SPINECRAFT LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2013
Days to Decision
210 days
Submission Type
Summary