FDA 510(k) FDA class 2 Substantially Equivalent for Some Indications 🇬🇧 United Kingdom

PRODEK

K Number: K953609 · Decision Jan 31, 1996
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
11
Review Days
182

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Basic Information

Device Name
PRODEK
K Number
K953609
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent for Some Indications
Applicant
Sutures , Ltd.
Date Received
August 2, 1995
Decision Date
January 31, 1996
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

Similar 510(k) Clearances

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

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Other Clearances by Sutures , Ltd.

K Number Device Name
K990432 SURGISORB
K943216 SURGIDEK
K943222 SURGIDEK S
K943218 CHROMIC CATGUT
K943223 SURGIDEK B
K943221 SURGIBOND
K943217 PLAIN CATGUT
K943627 SURGISILK
K943220 SUTULENE
K865038 SURGISTEEL
Search all 11 clearances from Sutures , Ltd. →