510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K902889Substantially Equivalent

A1-A,a1-B,a1-Abp,a1-Mbp,a1-Z,a6-A,a6-B,peh Pace.

BIOTRONIK AG, Lake Oswego OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902889 is the FDA 510(k) clearance record for A1-A,A1-B,A1-ABP,A1-MBP,A1-Z,A6-A,A6-B,PEH PACE., a class II device, cleared for Biotronik, GmbH & Co. on under FDA product code DTD (Pacemaker Lead Adaptor). FDA records list 104 510(k) clearances for Biotronik, GmbH & Co., from to . As of , FDA records show no recalls naming K902889.

Clearance record

Decision date
Received
(52 days to decision)
Product code
DTD Pacemaker Lead Adaptor
Regulation
21 CFR 870.3620
Device class
Class II
Review panel
Cardiovascular
Applicant
Biotronik, GmbH & Co. 6024 Southwest Jean Rd., Lake Oswego OR
Third party review
No

Clearances, product code DTD

Trailing 12 months

FDA records hold no clearances under product code DTD in the trailing twelve months.

FDA records show no clearances under product code DTD in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DTD, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260