Arthro Kinetics: FDA approves endoscopic instrumentation

By Lisa Kerner

Charlotte, N.C., Sept. 7 - The Food and Drug Administration granted 510(k) approval for Arthro Kinetics plc's endoscopic instrumentation, including the endoscope, instruments, light source and camera for use in minimally invasive spinal surgery (MISS).

The company plans to market the instrumentation immediately and is preparing additional FDA applications for other components in its MISS product range.

Arthro Kinetics is a medical device company located in Stuttgart, Germany.

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