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ARTHREX PROSTOP PLUS ARTHROEREISIS SUBTALAR IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K071456
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2008
Days to Decision
237 days
Submission Type
Summary

ARTHREX PROSTOP PLUS ARTHROEREISIS SUBTALAR IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K071456
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2008
Days to Decision
237 days
Submission Type
Summary