MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350— 510(k) K873710

Name: FDA 510(k) clearance K873710
Creator: U.S. Food and Drug Administration
Published: 1987-11-02

Substantially Equivalent

Arthropedics, Inc.

FDA 510(k) clearance K873710 for MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350, Substantially Equivalent on 1987-11-02. Applicant: Arthropedics, Inc.. Device class: 1.

Clearance details

Applicant: Arthropedics, Inc.
Product code: Code HWB
Device class: Class 1
Regulation: 21 CFR 888.4540
Advisory panel: Orthopedic
Date received: 1987-09-15
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallington, NJ, US

Download summary PDF View on FDA.gov ↗

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K870844 — SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR1987-03-13
K870083 — FERRAY EXTRACTOR1987-02-26
K801327 — THE EXTRACTOR I TM1980-06-09
K780300 — HIP PLATE REMOVAL INSTRUMENT1978-02-28

More clearances from Arthropedics, Inc.

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K873619 — ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)1988-01-14
K873653 — MONOPOLAR CAUTERY BLADE TIP #TM-17011987-12-15
K873654 — MONOPOLAR CAUTERY CONICAL TIP #TM-17021987-12-15
K873655 — MONOPOLAR CAUTERY RETROGADE TIP #TM-17031987-12-15
K873387 — VIDEO ARTHROSCOPE, 1.7MM X 55 MM1987-11-25

Adverse events under product code HWB

product code HWB

Malfunction: 1,893
Total: 1,893

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.