My guess is that even in spite of having used ReCell for compassionate use and/or by participating in clinical trials, hospitals still have to follow the usual protocol and review process before adopting a new treatment/device into their everyday use. Avita mentioned from the very beginning that they expected most burn centers would complete this review process (taking up to ~6 months) before making purchases. I'm guessing the 19 centers that made purchases soon after approval were able to fast track their internal reviews or had less internal "red tape" to deal with.
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