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AESCULAP CASPAR PLATE & SCREW SYSTEM FOR ANTERIOR CERVICAL FUSION

Page Type
Cleared 510(K)
510(k) Number
K953720
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/2/1995
Days to Decision
85 days
Submission Type
Summary

AESCULAP CASPAR PLATE & SCREW SYSTEM FOR ANTERIOR CERVICAL FUSION

Page Type
Cleared 510(K)
510(k) Number
K953720
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/2/1995
Days to Decision
85 days
Submission Type
Summary