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

DynaNail Mini Tapered Hybrid

K Number: K240530 · Decision Mar 21, 2024
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
16
Review Days
27

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Basic Information

Device Name
DynaNail Mini Tapered Hybrid
K Number
K240530
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MedShape, Inc.
Date Received
February 23, 2024
Decision Date
March 21, 2024
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HWC), 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
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
K141420 FASTFORWARD
Search all 16 clearances from MedShape, Inc. →