Chorus DDD Pacemaker

No FDA recalls found in the data synced 22 Oct 2026.

Full name

Non-Rate Responsive Pacemakers

Trade Name

Chorus Ddd Pacemaker

Generic Name

Implantable pulse generator, pacemaker (non-CRT)

FDA applicant

MicroPort CRM S.r.l.

PMA Number

P900022 ↗

FDA Product Code

LWP

Device Class

Class III

Advisory Committee

Cardiovascular

FDA Decision

APPR Approved

• VEGA Steroid-Eluting Endocardial Leads (VEGA™ R45, VEGA™ R52, and VEGA™ R58)

  Class III

  FDA PMA P130010 Active Approved 17 May 2023

• Angeion Sentinel Implantable Cardioverter Defibrillator (Icd)System and the Angeflex Tm Defibrillation Lead System.

  Class III

  FDA PMA P970024 Withdrawn Approved 19 Aug 1998

• Paradym CRT-D; Paradym RF CRT-D (ZL101), (ZL102); Intensia CRT-D; Platinium CRT-D 1711, 1741.

  Class III

  FDA PMA P060027 Active Approved 15 May 2008

• Stelix II Endocardial Pacing Leads

  Class III

  FDA PMA P020030 Active Approved 17 Jun 2004

• Ovatio Vr/Dr

  Class III

  FDA PMA P980049 Active Approved 15 Sep 1999

• SMARTVIEW hotspot

  Class III

  FDA PMA P950029 Active Approved 10 Mar 1997

• What type of device is the Chorus DDD Pacemaker?

  The Chorus DDD Pacemaker is an implantable pulse generator for non-CRT pacing, as defined by its generic name and device classification in the provided specifications.

• Who manufactures the Chorus DDD Pacemaker?

  The Chorus DDD Pacemaker is manufactured by MicroPort CRM USA, Inc., as stated in the manufacturer and applicant fields of the device data.

• What regulatory authorization applies to the Chorus DDD Pacemaker?

  The Chorus DDD Pacemaker has received FDA PMA authorization, as indicated by the AUTHORIZATIONS field and the PMA number P900022 in the specifications.