Last synced on 14 November 2025 at 11:06 pm

ARCHON ANTERIOR CERVICAL PLATE SYSTE,

Page Type
Cleared 510(K)
510(k) Number
K122910
510(k) Type
Special
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2012
Days to Decision
20 days
Submission Type
Summary

ARCHON ANTERIOR CERVICAL PLATE SYSTE,

Page Type
Cleared 510(K)
510(k) Number
K122910
510(k) Type
Special
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2012
Days to Decision
20 days
Submission Type
Summary