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HEDROCEL REVISION CUP, MODEL 02-2YY-ZZZZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001759
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2000
Days to Decision
76 days
Submission Type
Summary

HEDROCEL REVISION CUP, MODEL 02-2YY-ZZZZ

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001759
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2000
Days to Decision
76 days
Submission Type
Summary