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SUB-VENT (TM) IMPLANT/ENDOSSEOUS BLADE IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861425
510(k) Type
Traditional
Applicant
CORE-VENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1986
Days to Decision
203 days

SUB-VENT (TM) IMPLANT/ENDOSSEOUS BLADE IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861425
510(k) Type
Traditional
Applicant
CORE-VENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1986
Days to Decision
203 days