Last synced on 14 November 2025 at 11:06 pm

ARDIS INTERBODY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131242
510(k) Type
Traditional
Applicant
ZIMMER SPINE, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2013
Days to Decision
125 days
Submission Type
Summary

ARDIS INTERBODY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131242
510(k) Type
Traditional
Applicant
ZIMMER SPINE, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2013
Days to Decision
125 days
Submission Type
Summary