OMNIFIT CERAMIC MORSE TAPER HEAD (1002 SERIES)— 510(k) K885102

Name: FDA 510(k) clearance K885102
Creator: U.S. Food and Drug Administration
Published: 1989-06-22

Substantially Equivalent for Some Indications

Osteonics Corp.

FDA 510(k) clearance K885102 for OMNIFIT CERAMIC MORSE TAPER HEAD (1002 SERIES), Substantially Equivalent for Some Indications on 1989-06-22. Applicant: Osteonics Corp.. Device class: 2.

Clearance details

Applicant: Osteonics Corp.
Product code: Code LZO
Device class: Class 2
Regulation: 21 CFR 888.3353
Advisory panel: Orthopedic
Date received: 1988-12-12
Decision date: 1989-06-22
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Allendale, NJ, US

Download summary PDF View on FDA.gov ↗

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K983657 — OSTEONICS SERIES 7000 AD TIBIAL TRAY2000-04-06
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K984375 — OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLY1999-04-30
K982798 — OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEM1999-03-25
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Adverse events under product code LZO

product code LZO

Death: 17
Injury: 12,942
Malfunction: 1,756
Total: 14,715

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.