Last synced on 14 November 2025 at 11:06 pm

ARCOFIX

Page Type
Cleared 510(K)
510(k) Number
K080020
510(k) Type
Traditional
Applicant
SYNTHES SPINE CO.LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
141 days
Submission Type
Summary

ARCOFIX

Page Type
Cleared 510(K)
510(k) Number
K080020
510(k) Type
Traditional
Applicant
SYNTHES SPINE CO.LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
141 days
Submission Type
Summary