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ARCHON ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131025
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2013
Days to Decision
229 days
Submission Type
Summary

ARCHON ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131025
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/2013
Days to Decision
229 days
Submission Type
Summary