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

WATSON-FARRAR TOTAL HIP REPLACEMENT

K Number: K770219 · Decision Feb 17, 1977
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
58
Applicant Total
45
Review Days
14

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Basic Information

Device Name
WATSON-FARRAR TOTAL HIP REPLACEMENT
K Number
K770219
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Orthopedic Equipment Co., Inc.
Date Received
February 3, 1977
Decision Date
February 17, 1977
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 Orthopedic Equipment Co., Inc.

K Number Device Name
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K800530 SCHLEIN TRI-SURFACE ANKLE
K781445 SPREADER
K790247 TOURNIQUET TEST GAGE
K790209 FILTER SYSTEM, ALTNER DISPOSABLE
K781450 DRIVERS
K781444 OUTRIGGER DISTRACTION UNIT
K781451 FLAT WRENCH
K781447 THREADED ROD CLAMP
Search all 45 clearances from Orthopedic Equipment Co., Inc. →