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2.7MM LCP ULNA OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113364
510(k) Type
Traditional
Applicant
SYNTHES (USA) PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2012
Days to Decision
106 days
Submission Type
Summary

2.7MM LCP ULNA OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113364
510(k) Type
Traditional
Applicant
SYNTHES (USA) PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2012
Days to Decision
106 days
Submission Type
Summary