FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OPUS SPEEDSTITCH SUTURE DEVICE

K Number: K042031 · Decision Oct 19, 2004
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
13
Review Days
83

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Basic Information

Device Name
OPUS SPEEDSTITCH SUTURE DEVICE
K Number
K042031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Opus Medical, Inc.
Date Received
July 28, 2004
Decision Date
October 19, 2004
Product Code
GAT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GAT), ordered by most recent decision date.

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Other Clearances by Opus Medical, Inc.

K Number Device Name
K042584 OPUS MINIMAGNUM ANCHOR WITH INSERTER
K042914 OPUS MAGNUM KNOTLESS ANCHOR WITH INSERTER HANDLE
K041440 OPUS MAGNUM ANCHOR WITH INSERTER
K033317 SMARTSTITCH M-CONNECTOR, MODEL OM-8700; NEEDLE CASSETTE, OM-8750; AUTOCUFF SYSTEM INSTRUMENT SET, OM-9070
K030170 REUSABLE SMARTSTITCH SUTURE DEVICE, MODELS OM-8007, OM-8500
K031083 OPUS MAGNUM IMPLANT SYSTEM, MODEL OM-1500
K030235 F1 DIODE LASER SYSTEM
K023843 SMARTSTITCH M-CONNECTOR, MODEL OM-8005; SMARTSTITCH ACTUATION HANDLE, MODEL OM-8500; AND SMARTSTITCH SUTURE CARTRIDGE
K022229 SMARTSTITCH SUTURE DEVICE, MODEL OM-8500
K020172 OPUS MAGNUM ANCHOR & INSTRUMENT SET
Search all 13 clearances from Opus Medical, Inc. →