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ORTHOPILOT NEXT GENERATION-UKA SOFTWARE, MODEL FS210

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090375
510(k) Type
Traditional
Applicant
Aesculap Implant System, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2009
Days to Decision
126 days
Submission Type
Summary

ORTHOPILOT NEXT GENERATION-UKA SOFTWARE, MODEL FS210

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090375
510(k) Type
Traditional
Applicant
Aesculap Implant System, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2009
Days to Decision
126 days
Submission Type
Summary