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

METHA SHORT STEM HIP SYSTEM; MODULAR HIP SYSTEM; EXCIA HIP SYSTEM

K Number: K081973 · Decision Aug 7, 2008
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
22
Review Days
28

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Basic Information

Device Name
METHA SHORT STEM HIP SYSTEM; MODULAR HIP SYSTEM; EXCIA HIP SYSTEM
K Number
K081973
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, Inc.
Date Received
July 10, 2008
Decision Date
August 7, 2008
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, Inc.

K Number Device Name
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K111122 AESCULAP SIBD XP SPINAL SYSTEM
K103284 LAMINOPLASY PLATING SYSTEM
K100802 AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM
K092143 EXCIA TOTAL HIP SYSTEM M AN ML FEMORAL STEM
K083004 MILI (MINIMALLY INVASIVE LUMBAR IMPLANT) SYSTEM
K083311 AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM
Search all 22 clearances from Aesculap Implant Systems, Inc. →