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

22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD

K Number: K970846 · Decision Jun 5, 1997
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
15
Review Days
90

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
22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD
K Number
K970846
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Landos, Inc.
Date Received
March 7, 1997
Decision Date
June 5, 1997
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Similar 510(k) Clearances

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

View all

Other Clearances by Landos, Inc.

K Number Device Name
K964226 MEMORY STAPLE (20 SIZES AVAILABLE)
K971069 TWIST-OFF (TM) SCREW
K971070 SCARF THREAD-HEAD (TM) HEAD SCREW
K971068 34MM SCARF THREAD-HEAD(TM) SCREW
K961732 KAR
K953111 CORAIL
K962233 TWIST-OFF SCREW
K962236 SCARF THREAD-HEAD SCREW
K960642 NANCY NAIL
K943727 BIOSTOP G BONE CEMENT RESTRICTOR
Search all 15 clearances from Landos, Inc. →