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

Excia Total Hip System

K Number: K150062 · Decision Feb 9, 2015
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
22
Review Days
27

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Basic Information

Device Name
Excia Total Hip System
K Number
K150062
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap Implant Systems, LLC
Date Received
January 13, 2015
Decision Date
February 9, 2015
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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Other Clearances by Aesculap Implant Systems, LLC

K Number Device Name
K213871 Ennovate Cervical Spinal and Occiput System
K210963 ENNOVATE Spinal System
K180433 ENNOVATE®
K162134 ENNOVATE Spinal System
K153700 Aesculap(R) Implant Systems (AIS) S4 Navigation Instruments
K153396 Aesculap OrthoPilot Next Generation
K151938 S4 Cervical Spinal and Occiput Systems
K151056 Aesculap T-Space PEEK and XP Spinal System
K150544 Columbus Total Knee System, Columbus Revision Knee System, EnduRo Knee System
K141694 AESCULAP ORTHOPILOT NEXT GENERATION
Search all 22 clearances from Aesculap Implant Systems, LLC →