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

Infinity-Lock 3, Infinity-Lock 5

K Number: K171680 · Decision Jun 30, 2017
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
9
Review Days
24

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Basic Information

Device Name
Infinity-Lock 3, Infinity-Lock 5
K Number
K171680
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xiros, Ltd.
Date Received
June 6, 2017
Decision Date
June 30, 2017
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 Xiros, Ltd.

K Number Device Name
K230671 Pitch PaSoft Tissue Reinforcement Device
K222978 Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device
K220091 Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device
K220906 SECURE-LOCK
K211563 Pitch-Patchs
K191053 Xtreme-Loop
K180243 Infinity-Lock Button System
K151601 SECURE-LOOP