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

SEATTLE II TOTAL HIP SYSTEM

K Number: K812669 · Decision Oct 2, 1981
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
58
Applicant Total
13
Review Days
11

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Basic Information

Device Name
SEATTLE II TOTAL HIP SYSTEM
K Number
K812669
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Hexcel Medical
Date Received
September 21, 1981
Decision Date
October 2, 1981
Product Code
JDG
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
JDG Prosthesis, Hip, Femoral Component, Cemented, Metal

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Other Clearances by Hexcel Medical

K Number Device Name
K840416 HEXCELITE
K820890 URETHANE ORTHOPAEDIC CASTING TAPE
K812687 BRIGHAM II TOTAL HIP SYSTEM
K812068 PROPOSED CONTROLS FOR DOSIMETRIC RELEASE
K811164 URETHANE ORTHOPAEDIC CASTING TAPE
K810956 MARCOVE HUMERAL ROD
K810957 MARCOVE INTRAMEDULLARY ROD
K810230 CONDYLAR KNEE W/METAL ENCAPSULATED TIB
K800051 HEXCEL FEMORAL COMPONENT HIP PROSTHESIS
K800050 ANITOMIC TOTAL HIP SYSTEM
Search all 13 clearances from Hexcel Medical →