FDA Device Intelligence
Home › Ascension Orthopedics, Inc. › Ascension® First Choice® DRUJ System

Ascension® First Choice® DRUJ System

Ascension Orthopedics, Inc. · Model MUH600S55LWW · UDI-DI 10381780120728

KXE Prescription
1
510(k) clearances
45
Adverse events
3
Recalls
18
Facilities

Description

Ulnar Implant, Head

Recalls

DateFirmReason
2015-06-24Stryker Howmedica Osteonics Corp.Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum because packaging integrity (sterile barrier) of the packaging type KIT I may potentially be compromise
2015-06-24Stryker Howmedica Osteonics Corp.Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum because packaging integrity (sterile barrier) of the packaging type KIT I may potentially be compromise
2011-12-03Ascension Orthopedics, IncA recent review conducted by Ascension Orthopedics revealed that certain modifications were made to the First Choice System and should have been preceded by a submission of a filin

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
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.