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

VARI-ANGLE HIP SCREW (VHS) SYSTEM

K Number: K964880 · Decision Oct 16, 1997
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
5
Review Days
315

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Basic Information

Device Name
VARI-ANGLE HIP SCREW (VHS) SYSTEM
K Number
K964880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Walter Abendschein, M.D.
Date Received
December 5, 1996
Decision Date
October 16, 1997
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.

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Other Clearances by Walter Abendschein, M.D.

K Number Device Name
K011603 VHS PEDIATRIC HIP SCREW SYSTEM
K002184 COD COMPRESSION OSTEOTOMY DEVICE
K000827 UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTED
K991806 VHS SUPRACONDYLAR PLATE SYSTEM