ORTHOPEDIC SCREW FIXATION— 510(k) K932350

Name: FDA 510(k) clearance K932350
Creator: U.S. Food and Drug Administration
Published: 1995-07-05

Substantially Equivalent

Osteomed Corp.

FDA 510(k) clearance K932350 for ORTHOPEDIC SCREW FIXATION, Substantially Equivalent on 1995-07-05. Applicant: Osteomed Corp.. Device class: 2.

Clearance details

Applicant: Osteomed Corp.
Product code: Code HWC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1993-05-14
Decision date: 1995-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Wayne, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HWC

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K261057 — ActivaScrew Cannulated COM2026-09-04
K260106 — OsteoCoil GT Active Compression System2026-08-24
K262344 — Large Compression Screws2026-08-12
K253858 — GFS - Sterile Screws and Top Hat2026-08-05
K262075 — Lapidus Screw Kit2026-07-22

More clearances from Osteomed Corp.

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K151021 — OsteoMed Cannulated Screw System2015-07-15
K022277 — OSTEOMED CRANIAL FLAP FIXATION SYSTEM2003-04-01
K022887 — INTERPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM2002-11-26
K022886 — METATARSOPHALANGEAL FLEXIBLE STABILIZING ROD SYSTEM2002-11-25
K023260 — 1.2MM OSTEOMED AUTO-DRIVE SCREW SYSTEM2002-10-18

Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.