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AESCULAP SIBD XP SPINAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111122
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2011
Days to Decision
105 days
Submission Type
Summary

AESCULAP SIBD XP SPINAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111122
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2011
Days to Decision
105 days
Submission Type
Summary