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

DynaClipTM Bone Staple

K Number: K181781 · Decision Nov 5, 2018
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
16
Review Days
125

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Basic Information

Device Name
DynaClipTM Bone Staple
K Number
K181781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MedShape, Inc.
Date Received
July 3, 2018
Decision Date
November 5, 2018
Product Code
JDR
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
JDR Staple, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDR), ordered by most recent decision date.

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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
K171376 DynaNail TTC Fusion System
K141420 FASTFORWARD
Search all 16 clearances from MedShape, Inc. →