Using light and serial electron microscopy, we show profound refinements in motor axonal branching and synaptic connectivity before and after birth. Embryonic axons become maximally connected just before birth when they innervate ∼10-fold more muscle fibers than in maturity. In some developing muscles, axons innervate almost every muscle fiber. At birth, each neuromuscular junction is coinnervated by approximately ten highly intermingled axons (versus one in adults). Extensive die off of terminal branches occurs during the first several postnatal days, leading to much sparser arbors that still span the same territory. Despite the extensive pruning, total axoplasm per neuron increases as axons elongate, thicken, and add more synaptic release sites on their remaining targets. Motor axons therefore initially establish weak connections with nearly all available postsynaptic targets but, beginning at birth, massively redistribute synaptic resources, concentrating many more synaptic sites on many fewer muscle fibers. Analogous changes in connectivity may occur in the CNS. Display omitted ► Pervasive axonal pruning in the mouse neuromuscular system during early development ► Pruning occurs by removal of terminal as opposed to proximal branches ► At the peak, target cells are innervated by up to ∼10 axons with none dominant ► At peak, there is nearly all-to-all pre- to postsynaptic connectivity Synaptic connectivity between neurons and muscle fibers changes dramatically during development. Here, Tapia et al. show that nerve-muscle connections peak just before birth with a nearly all-to-all connectional pattern that is trimmed 10-fold after birth when axons focus more synaptic sites on far fewer targets.