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

HSS FEMORAL COMPONENTS

K Number: K934857 · Decision Jul 18, 1995
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
3
Review Days
644

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Basic Information

Device Name
HSS FEMORAL COMPONENTS
K Number
K934857
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hospital For Special Surgery
Date Received
October 12, 1993
Decision Date
July 18, 1995
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

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

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Other Clearances by Hospital For Special Surgery

K Number Device Name
K942032 PLAMP, PLAMP PLATE, PLAMP WITH HOOK
K935080 INSALL-BURSTEIN II