Last synced on 25 January 2026 at 3:41 am

AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100802
510(k) Type
Traditional
Applicant
Aesculap Implant Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2010
Days to Decision
120 days
Submission Type
Summary

AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100802
510(k) Type
Traditional
Applicant
Aesculap Implant Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2010
Days to Decision
120 days
Submission Type
Summary