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FIXEL EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K923032
510(k) Type
Traditional
Applicant
AMP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1993
Days to Decision
468 days
Submission Type
Summary

FIXEL EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K923032
510(k) Type
Traditional
Applicant
AMP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1993
Days to Decision
468 days
Submission Type
Summary