“…25,28,29 Factors influencing the degradation rate include the chemical identity of the monomeric constituents, the molecular weight distribution, crystallinity, size and shape of the implant, the implant site environment (intraosseous vs. soft tissue and degree of vascularity), and the metabolic condition of the recipient. 24,28,29 Many experimental studies of the degradation characteristics of bioabsorbable fixation implants are performed under in vitro 30 -33 or in vivo 16,19,20,23 conditions, but it is less common for the two methods to be employed simultaneously. 34,35 The devices investigated in this study were the Pop Rivet (Arthrotek, Inc., Warsaw, IN), made of a PGA/PLLA copolymer called LactoSorb (Biomet, Inc., Warsaw, IN), and the Suretac (Smith ϩ Nephew/Acufex Microsurgical, Inc., Northwood, MA), made of a glycolic acid/trimethylene carbonate copolymer called polyglyconate.…”