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

EXTERNAL FIXATION SYSTEMS

K Number: K031181 · Decision Jul 14, 2003
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
423
Review Days
90

Basic Information

Device Name
EXTERNAL FIXATION SYSTEMS
K Number
K031181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SMITH & NEPHEW, INC.
Date Received
April 15, 2003
Decision Date
July 14, 2003
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Similar 510(k) Clearances

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

View all

Other Clearances by SMITH & NEPHEW, INC.

K Number Device Name
K162996 INVISIKNOT Ankle Syndesmosis Repair Kit
K163086 VLP MINI-MOD 2.0mm Column Plates
K161233 OXINIUM DH Fermoral Heads
K161264 TRIGEN Low Profile Bone Screws
K162078 EVOS Small Fragment Plating System
K160923 REDAPT Anteverted Cemented Liner
K161665 VLP Wrist Fracture System
K152163 RENASYS GO
K160738 ZUK Select Knee System
K152566 PEBA Anchor/Suture Combination, 2.0mm Mini-Tac Anchor, Model 10-1629-01, Modification to Twinfix Ti Quick-T, Twinfix FT PK, Twinfix Ultra Ti, Twinfix Ultra PK, Twinfix Ultra HA Suture Anchors, FOOTPRINT Ultra OK Suture Anchors, BIORAPTOR 2.9 Suture Anchor, BIORAPTOR 2.3 PK Suture Anchor, OSTEORAPTOR Suture Anchor, BIORAPTOR Knotless Suture Anchor, HEALICOIL PK Suture Anchor (formerly Next Generation Fully Threaded Suture Anchor), Bioraptor Curved 2.3 PK Suture Anchors
Search all 423 clearances from SMITH & NEPHEW, INC. →