← DeviceClear
HomeDevice Clearances

ARTHREX FIBERWIRE IN USP SIZES — Arthrex, Inc. (510(k) K021434)

ARTHREX FIBERWIRE IN USP SIZES — Arthrex, Inc. (510(k) K021434) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ARTHREX FIBERWIRE IN USP SIZES; Applicant: Arthrex, Inc.; Clearance track: 510(k).

Device nameARTHREX FIBERWIRE IN USP SIZES
ApplicantArthrex, Inc.
Clearance track510(k)
Submission numberK021434
DecisionSubstantially Equivalent
Decision date2002-11-07
Date received2002-05-06
Product codeGAT
Device class2
Medical specialtyGeneral, Plastic Surgery
Applicant locationFL, US
SourceopenFDA device

🔍 Search all device clearances →