Atlas FDA

CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC

FDA 510(k) clearance K003028 · decided 2000-11-24

Clearance details

K-number
K003028
Device name
CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC
Applicant
Osteogenics Biomedical, Inc.
Decision
Substantially Equivalent
Date received
2000-09-28
Decision date
2000-11-24
Days to decision
57 days
Clearance type
Traditional
Product code
NBY
Device class
2
Regulation number
878.5035
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Lubbock, TX, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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Biotex (K180992)Purgo Biologics, Inc.2019-07-16
StitchKit (K191317)Origami Surgical2019-07-12
DemeTECH PTFE Nonabsorbable Surgical Suture (K181578)Demetech Corporation2018-10-11
PTFE SURGICAL SUTURE (K180630)Omnia Spa2018-04-06
C-PTFETM Surgical Suture (K173922)Cp Medical, Inc.2018-03-26
Gazelle PTFE and Suture Delivery Device (K173335)Dura Tap, LLC2018-02-08
WEGO-PTFE (K170842)Foosin Medical Supplies Inc., Ltd.2017-07-31
GOLNIT Non-Absorbable PTFE Surgical Suture (K163049)Antarma Dba Golnit Sutures2017-06-21
LS-5 ePTFE Suture (K163639)Lsi Solutions2017-06-02
LOOK PTFE Suture (K160744)Surgical Specialties Corporation2016-07-13

Recalls involving this device

No recalls on record reference this clearance.