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

MODIFICATION TO AEQUALIS SHOULDER FRACTURE SYSTEM

K Number: K003728 · Decision Dec 20, 2000
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
186
Applicant Total
44
Review Days
16

Basic Information

Device Name
MODIFICATION TO AEQUALIS SHOULDER FRACTURE SYSTEM
K Number
K003728
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TORNIER
Date Received
December 4, 2000
Decision Date
December 20, 2000
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.

View all

Other Clearances by TORNIER

K Number Device Name
K112144 AEQUALIS SHOULDER FRACTURE SYSTEM, AEQUALIS REVERSED SHOULDER PROSTHESIS, AEQUALIS REVERSED FRACTURE SHOULDER PROSTHESIS
K111970 KNEETEC PFJ&HLS KNEETEC PATELLAR COMPONENT
K111902 AEQUALIS SHOULDER SYSTEM
K094013 HLS KNEETEC SYSTEM
K100142 AEQUALIS REVERSED SHOULDER PROSTHESIS
K091870 TORNIER, PITON FIXATION IMPLANT SYSTEM
K090076 SALTO TALARIS TOTAL ANKLE PROSTHESIS
K082754 AEQUALIS HUMERAL NAIL SYSTEM
K082120 AEQUALIS REVERSED FRACTURE SHOULDER PROTHESIS
K081059 AEQUALIS REVERSED SHOULDER PROSTHESIS
Search all 44 clearances from TORNIER →