STRYKER CEMENT REMOVAL SYSTEM— 510(k) K961101

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K961101 for STRYKER CEMENT REMOVAL SYSTEM, Substantially Equivalent on 1996-07-15. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code LZV
Device class: Class 2
Regulation: 21 CFR 888.4580
Advisory panel: Orthopedic
Date received: 1996-03-19
Decision date: 1996-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LZV

K021502 — OSCAR, MODEL OE30002002-06-06
K930629 — ACRYL-X II SYSTEM1994-01-21
K904156 — ORIGIN(TM) CEMENT EXTRACT SYST STD-PR/SPL-PR KITS1990-11-27
K904180 — PROSTHETIC CEMENT REMOVER1990-11-20
K891472 — IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR1989-05-02

More clearances from Stryker Corp.

K230045 — HipCheck2023-09-29
K191259 — Stryker CrossFlow Integrated Arthroscopy Pump2019-07-12
K182359 — HipCheck2018-12-13
K143399 — Stryker Footed Attachments and Cutting Accessories2015-05-08
K143320 — Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments2015-04-23

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