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REPROCESSED EXTERNAL FIXATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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