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IMPLEX CONTINUUM KNEE SYSTEM: POROUS TIBIAL COMPONENT MODEL NUMBER 05-230 SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981560
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1998
Days to Decision
38 days
Submission Type
Summary

IMPLEX CONTINUUM KNEE SYSTEM: POROUS TIBIAL COMPONENT MODEL NUMBER 05-230 SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981560
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1998
Days to Decision
38 days
Submission Type
Summary