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INTERACTIVE/ SWISHPLUS2 IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130572
510(k) Type
Traditional
Applicant
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2013
Days to Decision
295 days
Submission Type
Summary

INTERACTIVE/ SWISHPLUS2 IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130572
510(k) Type
Traditional
Applicant
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2013
Days to Decision
295 days
Submission Type
Summary