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SCREW-VENT (TM) IMPLANT/ENDOSSEOUS SCREW IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K861426
510(k) Type
Traditional
Applicant
CORE-VENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1986
Days to Decision
174 days

SCREW-VENT (TM) IMPLANT/ENDOSSEOUS SCREW IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K861426
510(k) Type
Traditional
Applicant
CORE-VENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1986
Days to Decision
174 days