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

Taperloc® Complete Hip Stem

K Number: K251270 · Decision May 19, 2026
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
441
Review Days
390

Basic Information

Device Name
Taperloc® Complete Hip Stem
K Number
K251270
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet, Inc.
Date Received
April 24, 2025
Decision Date
May 19, 2026
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

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