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SILK SUTURES — Aurolab (510(k) K024091)

SILK SUTURES — Aurolab (510(k) K024091) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: SILK SUTURES; Applicant: Aurolab; Clearance track: 510(k).

Device nameSILK SUTURES
ApplicantAurolab
Clearance track510(k)
Submission numberK024091
DecisionSubstantially Equivalent
Decision date2003-02-28
Date received2002-12-11
Product codeGAP
Device class2
Medical specialtyGeneral, Plastic Surgery
Applicant locationWI, US
SourceopenFDA device

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