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KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974757
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/5/1998
Days to Decision
76 days

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974757
510(k) Type
Traditional
Applicant
ACROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/5/1998
Days to Decision
76 days