Last synced on 17 May 2024 at 11:06 pm

MODIFICATION TO SYNTHES (USA) CONDYLAR HEAD ADD-ON SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081747
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2008
Days to Decision
78 days
Submission Type
Summary

MODIFICATION TO SYNTHES (USA) CONDYLAR HEAD ADD-ON SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081747
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2008
Days to Decision
78 days
Submission Type
Summary