The AVEIR Leadless Pacemaker (LP)

Supplement S039 to premarket approval P150035. Product code PNJ. Decision 11 June 2026.

Approval

Each row is one field of the openFDA record. The grey name is the field’s name in openFDA’s documentation.

Field	Value	Field name
PMA number	P150035	pma_number
Supplement number	S039	supplement_number
Applicant	ABBOTT MEDICAL	applicant
Trade name	The AVEIR Leadless Pacemaker (LP)	trade_name
Generic name	Leadless pacemaker	generic_name
Product code	PNJ	product_code
Advisory committee	Cardiovascular	advisory_committee_description
Date received	2026-05-13	date_received
Decision date	2026-06-11	decision_date
Decision code	APPR	decision_code
Supplement type	Normal 180 Day Track No User Fee	supplement_type
Supplement reason	Postapproval Study Protocol	supplement_reason

Source: FDA openFDA, device/pma, P150035/S039, retrieved 2026-09-19 21:55 Eastern. Public domain (CC0).

Product code

The FDA classification record for the code on this record.

PNJ

Leadless Pacemaker

Device class 3 · Regulation 870.3610 · Review panel CV

All records with this codeClassification record on FDA

ArrHub vocabulary

Electrophysiology

PNJ is one of the 56 product codes in ArrHub’s electrophysiology vocabulary, each held with its FDA classification record as its citation. Vocabulary entry verified 20 September 2026.

Supplement history

Every record of this PMA number in ArrHub’s verified view, newest first. Routine notices are listed, never summarised away.

Record	Type	Reason	Decision
P150035 FDA	original approval	empty	2022-03-31
P150035/S041 FDA	Normal 180 Day Track	Change Design/Components/Specifications/Material	2026-08-27
P150035/S035 FDA	Normal 180 Day Track	Change Design/Components/Specifications/Material	2026-07-21
P150035/S040 FDA	30-Day Notice	Process Change - Manufacturer/Sterilizer/Packager/Supplier	2026-06-17
P150035/S039 FDA	Normal 180 Day Track No User Fee	Postapproval Study Protocol	2026-06-11
P150035/S038 FDA	Real-Time Process	Change Design/Components/Specifications/Material	2026-05-29
P150035/S037 FDA	Real-Time Process	Change Design/Components/Specifications/Material	2026-04-24
P150035/S036 FDA	Real-Time Process	Labeling Change - Indications/instructions/shelf life/tradename	2026-04-03
P150035/S034 FDA	Normal 180 Day Track No User Fee	Location Change - Manufacturer/Sterilizer/Packager/Supplier	2026-02-23
P150035/S026 FDA	135 Review Track For 30-Day Notice	Process Change - Manufacturer/Sterilizer/Packager/Supplier	2026-02-19

Source: FDA openFDA, device/pma, records of P150035, retrieved 2026-09-19 21:55 Eastern. 10 records in the verified view. Each identifier links to the FDA’s page.

ArrHub

What ArrHub adds to the record. Everything above this line is the agency’s; everything here is ArrHub’s, dated and attributed.

Record pair

No confirmed pair across the two registers for this record.

Resolved to

Abbott

The register name above is resolved to its organisation under ArrHub’s alias table. Method: rule:prefix. Source: fda_applicant. Verified 20 September 2026.

First seen by ArrHub’s weekly snapshot: 2026-09-20 08:40 Eastern.

Raw record

The stored record exactly as ArrHub holds it, for anyone who wants to check the page against it.

Show the raw record (JSON)device/pma.json?search=pma_number:P150035+AND+supplement_number:S039&limit=1

{
  "id": "09dd1b32-10a1-46db-a7b7-497259e6255b",
  "pma_key": "P150035/S039",
  "pma_number": "P150035",
  "supplement_number": "S039",
  "applicant": "ABBOTT MEDICAL",
  "trade_name": "The AVEIR Leadless Pacemaker (LP)",
  "generic_name": "Leadless pacemaker",
  "product_code": "PNJ",
  "advisory_committee_description": "Cardiovascular",
  "decision_date": "2026-06-11",
  "decision_code": "APPR",
  "supplement_type": "Normal 180 Day Track No User Fee",
  "supplement_reason": "Postapproval Study Protocol",
  "date_received": "2026-05-13",
  "source_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P150035&s=S039",
  "verified_at": "2026-09-20T01:57:11.963+00:00",
  "created_at": "2026-09-20T01:55:41.466163+00:00",
  "collected_at": "2026-09-20T01:55:27.157+00:00",
  "last_checked_at": null
}

The readable page is rendered from the record held in ArrHub’s verified view; the agency record at api.fda.gov governs where they differ.

Links open the agency’s own records. Unlabelled links open web pages. Links marked (JSON) open an agency’s data record, which a browser shows as plain text.

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