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

ORTHOLOC™ SPS Shoulder Plating System

K Number: K191711 · Decision Jul 17, 2019
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
51
Review Days
21

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Basic Information

Device Name
ORTHOLOC™ SPS Shoulder Plating System
K Number
K191711
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tornier, Inc.
Date Received
June 26, 2019
Decision Date
July 17, 2019
Product Code
HRS
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
HRS Plate, Fixation, Bone

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K Number Device Name
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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
K213124 Tomier Perform™ Reversed Glenoid Cannulated Glenospheres
K201315 PERFORM Humeral System – Stem
K193247 LATITUDE EV™ Total Elbow Arthroplasty
K191318 AEQUALIS FLEX REVIVE Shoulder System
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