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

ESKA-LIBUR HIP STEM

K Number: K053557 · Decision Jan 20, 2006
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
1
Review Days
30

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
ESKA-LIBUR HIP STEM
K Number
K053557
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eska Implants GmbH & Co.
Date Received
December 21, 2005
Decision Date
January 20, 2006
Product Code
LPH
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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Similar 510(k) Clearances

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

View all