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

AXYA SUTURE WELDING SYSTEM AND KIT

K Number: K070253 · Decision Jul 11, 2007
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
19
Review Days
166

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Basic Information

Device Name
AXYA SUTURE WELDING SYSTEM AND KIT
K Number
K070253
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
Axya Medical, Inc.
Date Received
January 26, 2007
Decision Date
July 11, 2007
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

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Other Clearances by Axya Medical, Inc.

K Number Device Name
K070773 AXYA, MODEL 3000 AXYZLOOP TITANIUM BONE ANCHOR
K063194 TUFFLEX POLYESTER SUTURE
K060165 AXYAFLEX POLYESTER SUTURE
K060970 AXYALOOP NONABSORBABLE BONE ANCHOR
K052491 AXYA MODEL 6500 AXYALOOP SELF-TAPPING BONE ANCHOR
K051983 MODEL 3000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
K051250 AXYA, MODEL 6500 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
K041698 AXYA MEDICAL, INC. MODEL 5000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
K022207 AXYA MODEL 3000 AXYALOOP TITANIUM BONE ANCHOR SYSTEM
K021929 AXYA MEDICAL, INC, MODEL 100 SONIC SCALPEL ULTRASONIC SURGICAL SYSTEM
Search all 19 clearances from Axya Medical, Inc. →