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2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101536
510(k) Type
Traditional
Applicant
SYNTHES (USA) LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2010
Days to Decision
104 days
Submission Type
Summary

2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101536
510(k) Type
Traditional
Applicant
SYNTHES (USA) LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2010
Days to Decision
104 days
Submission Type
Summary