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

Trivicta™ Hip Stem

K Number: K233758 · Decision Mar 8, 2024
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
158
Applicant Total
45
Review Days
105

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Basic Information

Device Name
Trivicta™ Hip Stem
K Number
K233758
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Development Corp.
Date Received
November 24, 2023
Decision Date
March 8, 2024
Product Code
MEH
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
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Similar 510(k) Clearances

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

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Other Clearances by Ortho Development Corp.

K Number Device Name
K253161 Balanced Knee System TriMax Porous Femoral Components
K251052 Trivicta® Hip Stem
K242984 BKS Revision System
K242833 Legend® Acetabular Shell
K142146 IBIS PEDICLE SCREW SYSTEM
K132697 ENCOMPASS 10/12 HIP STEM
K133386 OVATION TRIBUTE HIP STEM; OVATION NARROW HIP STEM
K133449 KASM KNEE ARTICULATING SPACER MOLDS
K131022 OVATION 10/12 HIP STEM
K131337 BALANCED KNEE SYSTEM HIGH FLEX VITAMIN E PS TIBIAL INSERT AND PATELLA
Search all 45 clearances from Ortho Development Corp. →