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VENUS ANTERIOR CERVICAL PLATE

Page Type
Cleared 510(K)
510(k) Number
K103137
510(k) Type
Traditional
Applicant
VERTICOR, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2011
Days to Decision
108 days
Submission Type
Summary

VENUS ANTERIOR CERVICAL PLATE

Page Type
Cleared 510(K)
510(k) Number
K103137
510(k) Type
Traditional
Applicant
VERTICOR, LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2011
Days to Decision
108 days
Submission Type
Summary