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ACROMED CABLE/WIRE PEDICLE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964007
510(k) Type
Traditional
Applicant
Acromed Corp.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/16/1996
Days to Decision
70 days

ACROMED CABLE/WIRE PEDICLE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964007
510(k) Type
Traditional
Applicant
Acromed Corp.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/16/1996
Days to Decision
70 days