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WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963587
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1997
Days to Decision
196 days
Submission Type
Summary

WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963587
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1997
Days to Decision
196 days
Submission Type
Summary