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

Tomier Perform™ Reversed Glenoid Cannulated Glenospheres

K Number: K213124 · Decision Oct 26, 2021
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
51
Review Days
29

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Basic Information

Device Name
Tomier Perform™ Reversed Glenoid Cannulated Glenospheres
K Number
K213124
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tornier, Inc.
Date Received
September 27, 2021
Decision Date
October 26, 2021
Product Code
PHX
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
PHX Shoulder Prosthesis, Reverse Configuration

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Other Clearances by Tornier, Inc.

K Number Device Name
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K230352 Tornier Humeral Nail and Tornier Long Humeral Nail
K220914 Tornier Perform Humeral System – Fracture
K220418 Tornier Perform Humeral System – Stemless
K211359 Tornier Perform™ Patient-Matched Primary Reversed Glenoid and BLUEPRINT™ Patient Specific Instrumentation
K201315 PERFORM Humeral System – Stem
K193247 LATITUDE EV™ Total Elbow Arthroplasty
K191711 ORTHOLOC™ SPS Shoulder Plating System
K191318 AEQUALIS FLEX REVIVE Shoulder System
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