Last synced on 25 April 2025 at 11:05 pm

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925682
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/7/1994
Days to Decision
427 days
Submission Type
Summary

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925682
510(k) Type
Traditional
Applicant
BIOPRO, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/7/1994
Days to Decision
427 days
Submission Type
Summary