Last synced on 30 May 2025 at 11:05 pm

SYNFIX-LR SPACER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072253
510(k) Type
Traditional
Applicant
SYNTHES SPINE CO.LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/2007
Days to Decision
59 days
Submission Type
Summary

SYNFIX-LR SPACER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072253
510(k) Type
Traditional
Applicant
SYNTHES SPINE CO.LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/2007
Days to Decision
59 days
Submission Type
Summary