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RESUBMITTED CLW ACETABULAR CUP W/SULMESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883794
510(k) Type
Traditional
Applicant
PROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1989
Days to Decision
261 days

RESUBMITTED CLW ACETABULAR CUP W/SULMESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883794
510(k) Type
Traditional
Applicant
PROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1989
Days to Decision
261 days