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

HOWMEDICA FEMORAL COMPONENT HIP SYS 6259

K Number: K851566 · Decision Jul 30, 1985
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
58
Applicant Total
373
Review Days
105

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Basic Information

Device Name
HOWMEDICA FEMORAL COMPONENT HIP SYS 6259
K Number
K851566
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Howmedica Corp.
Date Received
April 16, 1985
Decision Date
July 30, 1985
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

Similar 510(k) Clearances

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

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Other Clearances by Howmedica Corp.

K Number Device Name
K983528 MICRO DYNAMIC MESH
K983404 TYPE 3 FEMORAL COMPONENTS
K980925 DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION
K980926 DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION
K980632 DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION
K980626 DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
K983419 HOFFMANN II MIAMI POST
K982958 ZETA MULTIZONE LOCKING NAIL SYSTEM
K982873 ZETA MULTIZONE SCN LOCKING NAIL
K982531 HOWMEDICA LEIBINGER RESORBABLE FIXATION SYSTEM
Search all 373 clearances from Howmedica Corp. →