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MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K994205
510(k) Type
Traditional
Applicant
LIFECORE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2000
Days to Decision
90 days
Submission Type
Summary

MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K994205
510(k) Type
Traditional
Applicant
LIFECORE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/29/2000
Days to Decision
90 days
Submission Type
Summary