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ARTHREX INSTRUMENTS ( HIP )

Page Type
Cleared 510(K)
510(k) Number
K926212
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1994
Days to Decision
417 days
Submission Type
Statement

ARTHREX INSTRUMENTS ( HIP )

Page Type
Cleared 510(K)
510(k) Number
K926212
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1994
Days to Decision
417 days
Submission Type
Statement