This is a multicenter, prospective, retrospective, Post Market Clinical Follow-up (PMCF) study in subjects who have undergone or will undergo surgery utilizing one or more Stryker devices according to Stryker cleared Instructions for Use (IFU).
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S-S-102-A
Timeframe: Baseline through 24-months post-op.
S-S-102-B
Timeframe: Baseline through 24-months post-op.
S-S-102-C
Timeframe: Baseline through 24-months post-op.