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

BIOLOX OPTION CERAMIC FEMORAL HEAD AND METHA XL HEADS

K Number: K090299 · Decision Apr 24, 2009
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
7
Review Days
77

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Basic Information

Device Name
BIOLOX OPTION CERAMIC FEMORAL HEAD AND METHA XL HEADS
K Number
K090299
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
Date Received
February 6, 2009
Decision Date
April 24, 2009
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

Similar 510(k) Clearances

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

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Other Clearances by Aesculap Implant Systems

K Number Device Name
K140452 VEGA KNEE SYSTEM
K121879 VEGA KNEE SYSTEM
K101815 ENDURO KNEE SYSTEM
K100623 AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM
K090657 MODIFICATION TO: S4 SPINAL SYSTEM
K071945 S4 SPINAL SYSTEM