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

EXACTECH NOVATION CROWN CUP AND LINERS

K Number: K070479 · Decision Mar 15, 2007
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
186
Review Days
23

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Basic Information

Device Name
EXACTECH NOVATION CROWN CUP AND LINERS
K Number
K070479
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exactech, Inc.
Date Received
February 20, 2007
Decision Date
March 15, 2007
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

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Other Clearances by Exactech, Inc.

K Number Device Name
K260583 Equinoxe® Shoulder System
K250713 Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants
K243448 Equinoxe® Shoulder System
K243275 Equinoxe® Scapula Fracture System
K243839 Alteon® HA Femoral Stems
K240393 Exactech® TRULIANT® Knee System
K233482 Equinoxe® Central Screw Baseplate System
K230717 Exactech® Vantage® Total Ankle System
K223933 Exactech Equinoxe PHx Fracture System; Exactech EPIC Screws
K223833 Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter Trays
Search all 186 clearances from Exactech, Inc. →