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

V.E.P. HIP -VARIABLE ENDO-PROSTHESIS

K Number: K850928 · Decision May 28, 1985
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
106
Applicant Total
1
Review Days
84

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
V.E.P. HIP -VARIABLE ENDO-PROSTHESIS
K Number
K850928
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Unitas Ent.
Date Received
March 5, 1985
Decision Date
May 28, 1985
Product Code
KWL
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
KWL Prosthesis, Hip, Hemi-, Femoral, Metal

Similar 510(k) Clearances

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

View all