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| Article Library Discuss FDA panel rejects Zimmer spine implant in the General Discussion forums; FDA panel rejects Zimmer spine implant 11/4/2009, 3:11 p.m. CST MATTHEW PERRONE The Associated Press (AP) — GAITHERSBURG, Md. - ... |
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FDA panel rejects Zimmer spine implant
11/4/2009, 3:11 p.m. CST MATTHEW PERRONE The Associated Press (AP) — GAITHERSBURG, Md. - Federal health advisers on Wednesday rejected an implant from Zimmer Holdings saying it's unclear how effective or safe the device would be for treating a painful spinal condition. The Food and Drug Administration's panel of outside experts voted 5-1 that Zimmer's titanium Dynesys implant should not be approved to restabilize the spine. The FDA is not required to follow the group's recommendation, though it often does. A Zimmer study of the device met its goal, showing results at least as good as spinal fusion using the company's older Silhouette implant. Patients implanted with Dynesys showed a 52 percent treatment success rate after two years, compared with 40 percent for Silhouette. But panelists questioned the durability of the device beyond that time frame. "I'm worried about these screws having to last a lifetime," said panelist Dr. Edward Hanley of Carolinas Medical Center. Panelists said the Dynesys has potential as spine-stabilizing device, but would require a revamped study to better identify the ideal patient population. The FDA's review of the Dynesys implant was unusual in that it raised questions about whether company payments to physicians conducting the trial may have influenced the results. More than half of the patients in the trial were treated at medical centers that reported more than $100,000 in payments from the company, according to the FDA's review. While there was a relationship between the payments and whether patients achieved success with the device, the connection was not statistically significant. Panelists said the connection was likely due to chance. But FDA regulators said companies should expect to see increasing scrutiny of financial payments as part of product reviews. The FDA cited increasing interest from Congress in ties between device makers and surgeons. Sen. Charles Grassley, R-Iowa, is investigating device maker Medtronic Inc.'s consulting relationships with surgeons. The Minneapolis-based giant is a leading manufacturer of spinal repair products.
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Clinical trial participant disc c5-c6, Many artificial disc problems, Now fused C4-C7 with stem cells and plates |
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