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KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923703
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/20/1993
Days to Decision
300 days
Submission Type
Summary

KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923703
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/20/1993
Days to Decision
300 days
Submission Type
Summary