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

SUPERSTITCH GW, MODELS 06-15-04-GW, 08-15-04-GW

K Number: K053482 · Decision Dec 27, 2005
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
5
Review Days
13

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Basic Information

Device Name
SUPERSTITCH GW, MODELS 06-15-04-GW, 08-15-04-GW
K Number
K053482
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sutura, Inc.
Date Received
December 14, 2005
Decision Date
December 27, 2005
Product Code
GAW
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
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

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Other Clearances by Sutura, Inc.

K Number Device Name
K062125 SUPERSTITCH 5F, 12F, AND EL
K020940 SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X
K012865 SUPERSTITCH VASCULAR SUTURING DEVICE
K994087 SUPERSTITCH