NORMED TITANIUM RONDO FIX FUSION PLATES AND SCREW SYSTEM— 510(k) K022323

Name: FDA 510(k) clearance K022323
Creator: U.S. Food and Drug Administration
Published: 2002-09-09

Substantially Equivalent

Osteomedics, Inc.

FDA 510(k) clearance K022323 for NORMED TITANIUM RONDO FIX FUSION PLATES AND SCREW SYSTEM, Substantially Equivalent on 2002-09-09. Applicant: Osteomedics, Inc.. Device class: 2.

Clearance details

Applicant: Osteomedics, Inc.
Product code: Code HRS
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2002-07-17
Decision date: 2002-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paramus, NJ, US

Download summary PDF View on FDA.gov ↗

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More clearances from Osteomedics, Inc.

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K022035 — OSTEOMEDICS RESORBABLE SMALL FIXATION SYSTEM, OSTEOSORB2003-01-17
K022324 — NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM2002-09-17
K022231 — NORMED DISTAL RADIUS RECONSTRUCTION SYSTEM2002-09-13
K022230 — NORMED MINI EXTERNAL FIXATOR SYSTEM2002-09-10
K022325 — NORMED TITANIUM OSTEOTOMY PLATING SYSTEM2002-09-09

Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.