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AESCULAP PEEK CRANIOFIX

Page Type
Cleared 510(K)
510(k) Number
K091692
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2010
Days to Decision
428 days
Submission Type
Summary

AESCULAP PEEK CRANIOFIX

Page Type
Cleared 510(K)
510(k) Number
K091692
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2010
Days to Decision
428 days
Submission Type
Summary