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WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION)

Page Type
Cleared 510(K)
510(k) Number
K960978
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1996
Days to Decision
102 days
Submission Type
Summary

WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION)

Page Type
Cleared 510(K)
510(k) Number
K960978
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1996
Days to Decision
102 days
Submission Type
Summary