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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K161192

Wagner SL Revision Stem Lateral, Wagner Cone Prosthesis® System · Zimmer GmbH · decided 2016-07-08 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Wagner SL Revision®01.00109.015Zimmer GmbHJDI KWZ LPH LZO00889024277649
Wagner SL Revision®01.00109.023Zimmer GmbHJDI KWZ LPH LZO00889024277724
Wagner SL Revision®01.00109.019Zimmer GmbHJDI KWZ LPH LZO00889024277687
Wagner SL Revision®01.00109.024Zimmer GmbHJDI KWZ LPH LZO00889024277731
Wagner SL Revision®01.00109.022Zimmer GmbHJDI KWZ LPH LZO00889024277717
Wagner SL Revision®01.00109.017Zimmer GmbHJDI KWZ LPH LZO00889024277663
Wagner SL Revision®01.00109.025Zimmer GmbHJDI KWZ LPH LZO00889024277748
Wagner SL Revision®01.00109.014Zimmer GmbHJDI KWZ LPH LZO00889024277632
Wagner SL Revision®01.00109.016Zimmer GmbHJDI KWZ LPH LZO00889024277656
Wagner SL Revision®01.00109.018Zimmer GmbHJDI KWZ LPH LZO00889024277670
Wagner SL Revision®01.00109.021Zimmer GmbHJDI KWZ LPH LZO00889024277700
Wagner SL Revision®01.00109.020Zimmer GmbHJDI KWZ LPH LZO00889024277694