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KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV

Page Type
Cleared 510(K)
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)
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