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VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K050588
510(k) Type
Traditional
Applicant
INNOVATIVE SPINAL DESIGN, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2005
Days to Decision
44 days
Submission Type
Summary

VERTEVIEW ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K050588
510(k) Type
Traditional
Applicant
INNOVATIVE SPINAL DESIGN, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2005
Days to Decision
44 days
Submission Type
Summary