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

MONOSPHERICAL RESURFACING GLENOID PROS

K Number: K833409 · Decision Nov 7, 1983
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
68
Applicant Total
373
Review Days
38

Basic Information

Device Name
MONOSPHERICAL RESURFACING GLENOID PROS
K Number
K833409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3650
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
HOWMEDICA CORP.
Date Received
September 30, 1983
Decision Date
November 7, 1983
Product Code
KWT
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
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

Similar 510(k) Clearances

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

View all

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
K980626 DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
K980632 DURATION II TIBIAL INSERTS - 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. →