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

PSK POSTERIOR STABILIZED TOATAL KNEE

K Number: K915798 · Decision Mar 4, 1993
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
9
Review Days
436

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Basic Information

Device Name
PSK POSTERIOR STABILIZED TOATAL KNEE
K Number
K915798
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Implantology Corp.
Date Received
December 24, 1991
Decision Date
March 4, 1993
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.

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Other Clearances by Implantology Corp.

K Number Device Name
K934729 UFC HIP STEM COMPONENTS: HYDROXYLAPATITE COATED
K915529 FPC/SFPC/RFPC ACETABULAR COMPONENT
K915528 BHR BIPOLAR FEMORAL HEAD COMPONENT
K915527 CPS ACETABULAR COMPONENT
K915385 PPC HIP STEM COMPONENT
K924099 UFC HIP STEM COMPONENT
K915391 FPC HIP STEM COMPONENT
K915584 CRK CONDYLAR RESURFACING TOTAL KNEE