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ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K895267
510(k) Type
Traditional
Applicant
ARTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
230 days

ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K895267
510(k) Type
Traditional
Applicant
ARTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
230 days