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TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K914362
510(k) Type
Traditional
Applicant
ACORN GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1992
Days to Decision
211 days
Submission Type
Statement

TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K914362
510(k) Type
Traditional
Applicant
ACORN GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1992
Days to Decision
211 days
Submission Type
Statement