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

Taperloc® Complete Hip Stems

K Number: K200196 · Decision Dec 8, 2020
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
4
Review Days
316

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Basic Information

Device Name
Taperloc® Complete Hip Stems
K Number
K200196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Orthopedics
Date Received
January 27, 2020
Decision Date
December 8, 2020
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.

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Other Clearances by Biomet Orthopedics

K Number Device Name
K252404 Comprehensive Reverse Shoulder - HA Glenosphere Baseplates
K243761 A.L.P.S. Small Fragment Plating System
K223631 Comprehensive Segmental Revision System(SRS)