FDA Device Intelligence
HomeDevice types › NJL

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing

FDA product code NJL · Class 3 · Unknown

2,102
Registered devices
25,951
Adverse events
269
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-08-10DePuy Orthopaedics, Inc.Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may
2021-02-22DePuy Orthopaedics, Inc.Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+) Tibial Bases due to potential damaged packaging. These implant components are utili
2021-02-22DePuy Orthopaedics, Inc.Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+) Tibial Bases due to potential damaged packaging. These implant components are utili
2019-10-10Zimmer Biomet, Inc.Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.