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ORTHOPILOT NEXT GENERATION, MODEL FS101-FS106

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080547
510(k) Type
Special
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
85 days
Submission Type
Summary

ORTHOPILOT NEXT GENERATION, MODEL FS101-FS106

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080547
510(k) Type
Special
Applicant
AESCULAP IMPLANT SYSTEM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
85 days
Submission Type
Summary