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Long Term Supply of Osteocel(R) Plus Solidified Without Ownership of Processing Facility
Date:3/30/2009

(R), Osteocel Plus, and the Progentix products, all of which are intended to facilitate fusion and complement the core fixation products.

NuVasive cautions you that statements included in this press release that are not a description of historical facts are forward-looking statements that involve risks, uncertainties, assumptions and other factors which, if they do not materialize or prove correct, could cause NuVasive's results to differ materially from historical results or those expressed or implied by such forward-looking statements. The potential risks and uncertainties that could cause actual growth and results to differ materially include, but are not limited to: the risk that NuVasive revenue projections may prove incorrect because of unexpected difficulty in generating sales or achieving anticipated profitability; the risk that NuVasive may encounter unanticipated difficulty integrating the Osteocel product into its product line; the risk that NuVasive may be unable to generate expected revenues from Osteocel; the uncertain process of seeking regulatory approval or clearance for NuVasive's products of devices, including risks that such process could be significantly delayed; the possibility that the FDA may require significant changes to NuVasive's products or clinical studies; the risk that products may not perform as intended and may therefore not achieve commercial success; the risk that competitors may develop superior products or may have a greater market position enabling more successful commercialization; the risk that additional clinical data may call into question the benefits of NuVasive's products to patients, hospitals and surgeons; and other risks and uncertainties more fully described in NuVasive's press releases and periodic filings with the Securities and Exchange Commission. NuVasive's public filings with the Securities and Exchange Commission are available at www.sec.
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