510(k) Report

FDA applicant

Walter Abendschein, M.D.

Chevy Chase, MD5 decisions1997–20013 recalls

FDA records 5 decisions for Walter Abendschein, M.D. (Chevy Chase, MD) from 1997 to 2001: 5 510(k) clearances. Most are in product codes KTT (Appliance, Fixation, Nail/Blade/Plate…) and HRS (Plate, Fixation, Bone). 3 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Walter Abendschein, M.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Walter Abendschein, M.D. since 2007.

Recalls per year

1in 2016

2016: 1
2007high 1 (2016) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Walter Abendschein, M.D. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Walter”

FDA records each applicant name separately; these may or may not be the same firm.