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ARTECH TYPE SS SUBMERGED SCREW IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K891346
510(k) Type
Traditional
Applicant
ARTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1989
Days to Decision
286 days

ARTECH TYPE SS SUBMERGED SCREW IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K891346
510(k) Type
Traditional
Applicant
ARTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1989
Days to Decision
286 days