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IMPLEX CONTINUUM PATELLA-REVISION HEDROCEL PATELLA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983835
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1999
Days to Decision
136 days
Submission Type
Summary

IMPLEX CONTINUUM PATELLA-REVISION HEDROCEL PATELLA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983835
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1999
Days to Decision
136 days
Submission Type
Summary