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PRO-DENSE CORE DECOMPRESSION PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K072597
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2007
Days to Decision
31 days
Submission Type
Summary

PRO-DENSE CORE DECOMPRESSION PROCEDURE KIT

Page Type
Cleared 510(K)
510(k) Number
K072597
510(k) Type
Traditional
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2007
Days to Decision
31 days
Submission Type
Summary