Last synced on 30 May 2025 at 11:05 pm

LATERAL SYNFIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131276
510(k) Type
Traditional
Applicant
SYNTHES (USA) PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2014
Days to Decision
245 days
Submission Type
Summary

LATERAL SYNFIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131276
510(k) Type
Traditional
Applicant
SYNTHES (USA) PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2014
Days to Decision
245 days
Submission Type
Summary