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PRECISION OSTEOLOCK ACETABULAR COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K930275
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/1/1994
Days to Decision
590 days
Submission Type
Summary

PRECISION OSTEOLOCK ACETABULAR COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K930275
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
9/1/1994
Days to Decision
590 days
Submission Type
Summary