FDA Device Intelligence
HomeDevice types › NXT

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

FDA product code NXT · Class 3 · Unknown

280
Registered devices
6,885
Adverse events
6
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-07-14Smith & Nephew Orthopaedics Ltd. (Aurora)The nail head may become detached during surgery.
2018-05-11Smith & Nephew, Inc.The affected devices are manufactured to the same design specification as products intended for sale and use in the US but do not contain the FDA approved label
2018-05-11Smith & Nephew, Inc.The affected devices are manufactured to the same design specification as products intended for sale and use in the US but do not contain the FDA approved label
2015-06-03Smith & Nephew, Inc.The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had revision rates which were higher than established benchmarks.
2015-06-03Smith & Nephew, Inc.The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had revision rates which were higher than established benchmarks.
2015-06-03Smith & Nephew, Inc.The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had revision rates which were higher than established benchmarks.

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.