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Condylar Plate Fixation Implant
FDA product code JDP · Class 2 · Orthopedic
0
Registered devices
876
Adverse events
2
Recalls
2
510(k) clearances
Devices with this code
NA — Synthes GmbHNA — Synthes GmbHVA-LCP — SYNTHES (U.S.A.) LPVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDANA — Synthes GmbHVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDANA — SYNTHES (U.S.A.) LPVA-LCP — Synthes GmbHVA-LCP — Synthes GmbHVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDANA — SYNTHES (U.S.A.) LPVA-LCP — Synthes GmbHNA — Synthes GmbHVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDANA — Synthes GmbHVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVA-LCP — SYNTHES (U.S.A.) LPVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDAVersalock Periprosthetic Femur Plates System-GMReis — GM DOS REIS INDUSTRIA E COMERCIO LTDA
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-02-05 | Synthes, Inc. | Labeling correction: The package insert in one 5.0mm Variable Locking Screw package was a GP0006 (Anterior Cervical Vertebrae Plate System) insert, which should |
| 2013-05-29 | Synthes USA HQ, Inc. | A plate was inadvertently released to a sales consultant that was restricted for sale. |
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