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ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
510(k) Number
K873826
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1988
Days to Decision
434 days

ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
510(k) Number
K873826
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1988
Days to Decision
434 days