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AESCULAP IMPLANT SYSTEMS HIGH TIBIAL OSTEOTOMY PLATING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080992
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2008
Days to Decision
150 days
Submission Type
Summary

AESCULAP IMPLANT SYSTEMS HIGH TIBIAL OSTEOTOMY PLATING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080992
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2008
Days to Decision
150 days
Submission Type
Summary