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

ECLIPSE SOFT TISSUE FASTENER

K Number: K123350 · Decision Mar 7, 2013
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
16
Review Days
127

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Basic Information

Device Name
ECLIPSE SOFT TISSUE FASTENER
K Number
K123350
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MedShape, Inc.
Date Received
October 31, 2012
Decision Date
March 7, 2013
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 MedShape, Inc.

K Number Device Name
K254110 DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip Forte; DynaClip Delta; DynaClip Quattro
K250628 DynaNail TTC Fusion System
K240530 DynaNail Mini Tapered Hybrid
K220812 DynaClip® Bone Staple
K203595 DynaFuse Fixation System
K203381 Dynanail Mini Hybrid
K193305 DynaClip Bone Staple
K182677 DynaNail Mini
K181781 DynaClipTM Bone Staple
K171376 DynaNail TTC Fusion System
Search all 16 clearances from MedShape, Inc. →