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

PLASMA SPRAYED SHOULDER

K Number: K003324 · Decision Dec 6, 2001
Classifications
1
FEI Numbers
218
Registration Numbers
218
Same Product Code
189
Applicant Total
85
Review Days
408

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Basic Information

Device Name
PLASMA SPRAYED SHOULDER
K Number
K003324
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Orthopedics, Inc.
Date Received
October 24, 2000
Decision Date
December 6, 2001
Product Code
KWS
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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Similar 510(k) Clearances

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

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Other Clearances by Encore Orthopedics, Inc.

K Number Device Name
K032905 3DKNEE POROUS COATED FEMORAL COMPONENT
K020114 3D KNEE
K020741 UNICONDYLAR KNEE
K020236 MODIFICATION TO PASS SPINAL SYSTEM
K020170 KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP
K013490 CEMENTED CALCAR HIP SYSTEM
K013442 PASS SPINAL SYSTEM
K013431 PASS SPINAL SYSTEM
K013191 PASS SPINAL SYSTEM
K011856 RADIOGRAPHIC MARKERS
Search all 85 clearances from Encore Orthopedics, Inc. →