FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

SECULOK™ Suture Anchor

K Number: K180759 · Decision Aug 9, 2018
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
23
Review Days
140

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Basic Information

Device Name
SECULOK™ Suture Anchor
K Number
K180759
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
U&I Corporation
Date Received
March 22, 2018
Decision Date
August 9, 2018
Product Code
MBI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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Other Clearances by U&I Corporation

K Number Device Name
K220147 Aspiron S ACP System
K210573 Velofix SA Cervical Cage
K183243 Velofix TLIF Cage
K190067 Velofix Interbody Fusion System
K190053 SECULOK™ ACP System
K181824 CBT Screw Fixation System
K183383 ANAX™ OCT Spinal System
K181829 Velofix TLIF Cage
K182055 SECULOK™ ACP System
K173198 Facet Screw Fixation System
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