Last synced on 14 November 2025 at 11:06 pm

OPTON PRO

Page Type
Cleared 510(K)
510(k) Number
K141564
510(k) Type
Traditional
Applicant
ZIMMER MEDIZINSYSTEMS GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/24/2014
Days to Decision
134 days
Submission Type
Summary

OPTON PRO

Page Type
Cleared 510(K)
510(k) Number
K141564
510(k) Type
Traditional
Applicant
ZIMMER MEDIZINSYSTEMS GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/24/2014
Days to Decision
134 days
Submission Type
Summary