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REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K012623
510(k) Type
Traditional
Applicant
ALLIANCE MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2002
Days to Decision
315 days
Submission Type
Summary

REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K012623
510(k) Type
Traditional
Applicant
ALLIANCE MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/2002
Days to Decision
315 days
Submission Type
Summary