Last synced on 17 May 2024 at 11:06 pm

ORTHOPILOT HTO MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021327
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2002
Days to Decision
90 days
Submission Type
Summary

ORTHOPILOT HTO MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021327
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2002
Days to Decision
90 days
Submission Type
Summary