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

NEOTRACT ANCHOR

K Number: K061700 · Decision Oct 26, 2006
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
17
Review Days
132

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Basic Information

Device Name
NEOTRACT ANCHOR
K Number
K061700
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neotract, Inc.
Date Received
June 16, 2006
Decision Date
October 26, 2006
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 Neotract, Inc.

K Number Device Name
K232558 UroLift 2 ATC Advanced Tissue Control System
K212396 UroLift System Rigid Retrieval Kit Sterilization Tray
K201837 UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2 Implant Cartridge
K200441 UroLift Advanced Tissue Control (ATC) System
K192781 UroLift System Procedure Kit Sterilization Tray
K193269 UroLift System (UL400)
K190377 UroLift System UL400
K173087 UroLift System (UL400 and UL500)
K172359 UroLift System (UL500)
K162345 UroLift System UL500, UroLift Delivery Handle, UroLift Implant Cartiridge
Search all 17 clearances from Neotract, Inc. →