OSTEONICS ALL POLYETHYLENE GLENOID SHOULDER COMPONENT— 510(k) K950521

Name: FDA 510(k) clearance K950521
Creator: U.S. Food and Drug Administration
Published: 1995-06-16

Substantially Equivalent

Osteonics Corp.

FDA 510(k) clearance K950521 for OSTEONICS ALL POLYETHYLENE GLENOID SHOULDER COMPONENT, Substantially Equivalent on 1995-06-16. Applicant: Osteonics Corp.. Device class: 2.

Clearance details

Applicant: Osteonics Corp.
Product code: Code KWS
Device class: Class 2
Regulation: 21 CFR 888.3660
Advisory panel: Orthopedic
Date received: 1995-02-06
Decision date: 1995-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KWS

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K260721 — Tornier Perform Advanced Glenoid2026-07-22
K254084 — AETOS Shoulder System - CONCELOC Glenoids2026-04-06
K252418 — Catalyst F1x Shoulder System2025-11-06
K252416 — AETOS Shoulder System Meta Humeral Prosthesis Size 02025-10-29
K241292 — MyShoulder Planner (5.3SSWPL)2025-01-30

More clearances from Osteonics Corp.

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K983657 — OSTEONICS SERIES 7000 AD TIBIAL TRAY2000-04-06
K980070 — OSTEONICS HA-COATED DEVICES1999-07-23
K984375 — OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLY1999-04-30
K982798 — OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEM1999-03-25
K984585 — OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVE1999-02-24

Adverse events under product code KWS

product code KWS

Death: 6
Injury: 9,652
Malfunction: 1,385
Other: 1
Total: 11,044

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.