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QUINTEX CERVICAL PLATING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100243
510(k) Type
Traditional
Applicant
Aesculap Implant Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2010
Days to Decision
218 days
Submission Type
Summary

QUINTEX CERVICAL PLATING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100243
510(k) Type
Traditional
Applicant
Aesculap Implant Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2010
Days to Decision
218 days
Submission Type
Summary