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

Tornier Perform Humeral System – Stemless

K Number: K220418 · Decision Sep 14, 2022
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
18
Applicant Total
51
Review Days
212

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Basic Information

Device Name
Tornier Perform Humeral System – Stemless
K Number
K220418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tornier, Inc.
Date Received
February 14, 2022
Decision Date
September 14, 2022
Product Code
PKC
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
PKC Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-Constrained

Similar 510(k) Clearances

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

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Other Clearances by Tornier, Inc.

K Number Device Name
K252788 Tornier Perform™ Reversed Monopost Glenoid (Perform Mono)
K251686 Tornier Humeral Reconstruction System Max (Tornier HRS Max)
K230352 Tornier Humeral Nail and Tornier Long Humeral Nail
K220914 Tornier Perform Humeral System – Fracture
K211359 Tornier Perform™ Patient-Matched Primary Reversed Glenoid and BLUEPRINT™ Patient Specific Instrumentation
K213124 Tomier Perform™ Reversed Glenoid Cannulated Glenospheres
K201315 PERFORM Humeral System – Stem
K193247 LATITUDE EV™ Total Elbow Arthroplasty
K191711 ORTHOLOC™ SPS Shoulder Plating System
K191318 AEQUALIS FLEX REVIVE Shoulder System
Search all 51 clearances from Tornier, Inc. →