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

DEPUY PFC SIGMA KNEE PROSTHESIS

K Number: K060515 · Decision Mar 23, 2006
Classifications
1
FEI Numbers
320
Registration Numbers
320
Same Product Code
902
Applicant Total
194
Review Days
24

Basic Information

Device Name
DEPUY PFC SIGMA KNEE PROSTHESIS
K Number
K060515
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DEPUY ORTHOPAEDICS, INC.
Date Received
February 27, 2006
Decision Date
March 23, 2006
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

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

View all

Other Clearances by DEPUY ORTHOPAEDICS, INC.

K Number Device Name
K150862 DePuy Actis Duofox Hip Prosthesis
K132959 DEPUY PINNACLE ALTRX ACETABULAR LINERS
K122395 DEPUY AGILITY LP TOTAL ANKLE PROSTHESIS
K111663 TRAUMA INTERNAL FIXATION SYSTEMS
K112218 ACE-FISCHER(R), TEMPFIX(R), HOFFMAN CLASSIC(TM) EXTERNAL FIXATORS
K111433 DEPUY STTUNE (TM) PS KNEE SYSTEM
K110397 TRUMATCH PERSONALIZED SOLUTIONS
K111077 ORTHOSORB RESORBABLE PINS
K111444 UNIVERSAL AND TROCH ENTRY FEMORAL NAILING SYSTEMS LINE EXTENSION
K103756 DEPUY ATTUNE TOTAL KNEE SYSTEM
Search all 194 clearances from DEPUY ORTHOPAEDICS, INC. →