HWPClass I

Punch, Femoral Neck

21 CFR 888.4540 / Orthopedic

HWP is the FDA product code for Punch, Femoral Neck, a class I device type, regulated under 21 CFR 888.4540. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1987-03-13, and no recalls.

Classification record

Product code: HWP
Device name: Punch, Femoral Neck
Regulation: 21 CFR 888.4540
Device class: Class I
Review panel: Orthopedic
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code HWP

By decision year

1 clearance under product code HWP with a decision year between 1987 and 1987, 1987 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code HWP by decision year
Year	Clearances
1987	1

Applicants with the most clearances

Product code HWP

Applicants holding the most 510(k) clearances under product code HWP
Applicant	Clearances
Warsaw Orthopedic, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 41 companies shown, in name order

Recent clearances

Product code HWP

K870846Class ISchultz Mp Component PunchWarsaw Orthopedic, Inc. / cleared 1987-03-13

Recent recalls

Product code HWP

FDA records show no recalls under product code HWP.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)