Grappler® Interference Screw Post-Market Clinical Follow-Up Study

Inclusion Criteria: * The subject must have undergone a foot and/or ankle procedure involving soft tissue attachment to bone using the Grappler® Interference Screw System and completed by one of the designated investigators who are experienced in the use of such implants and the required specialized surgical techniques * The subject must have adequate radiographic and medical records for the minimum follow-up requirement of six months For the Prospective Data Collection: \- The subject is willing to provide written informed consent Exclusion Criteria: * None