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

HOFFMAN LEG LENGTHENING DEVICE

K Number: K802776 · Decision Nov 19, 1980
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
84
Applicant Total
373
Review Days
14

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Basic Information

Device Name
HOFFMAN LEG LENGTHENING DEVICE
K Number
K802776
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Howmedica Corp.
Date Received
November 5, 1980
Decision Date
November 19, 1980
Product Code
JEC
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
JEC Component, Traction, Invasive

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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. →