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HYDROXYAPATITE (HA) REFLECTION ACETABULAR SHELL, HYDROXYAPATITE (HA) REFLECTION INTERFIT SHELL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990666
510(k) Type
Abbreviated
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1999
Days to Decision
157 days
Submission Type
Summary

HYDROXYAPATITE (HA) REFLECTION ACETABULAR SHELL, HYDROXYAPATITE (HA) REFLECTION INTERFIT SHELL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990666
510(k) Type
Abbreviated
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1999
Days to Decision
157 days
Submission Type
Summary