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ACROMED ILIAC SCREW

Page Type
Cleared 510(K)
510(k) Number
K884161
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/3/1989
Days to Decision
211 days

ACROMED ILIAC SCREW

Page Type
Cleared 510(K)
510(k) Number
K884161
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/3/1989
Days to Decision
211 days