Last synced on 14 November 2025 at 11:06 pm

QUINTEX CERVICAL PLATING SYSTEM

Page Type
Cleared 510(K)
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)
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