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

VENTED CEMENT RESTRICTOR

K Number: K022729 · Decision Nov 14, 2002
Classifications
1
FEI Numbers
36
Registration Numbers
37
Same Product Code
22
Applicant Total
16
Review Days
90

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Basic Information

Device Name
VENTED CEMENT RESTRICTOR
K Number
K022729
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.4580
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amedica Corp.
Date Received
August 16, 2002
Decision Date
November 14, 2002
Product Code
JDX
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
JDX Instrument, Surgical, Sonic And Accessory/Attachment

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K142347 Amedica Valeo II Interbody Fusion Device
K121892 PHANTOM PLUS CERAMIC CAGE SYSTEM
K091278 VALEO SPACER SYSTEM
K082037 SEEPLATE CERVICAL PLATE SYSTEM
K073430 VALEO PEDICLE SCREW SPINAL SYSTEM
K073505 MODIFICATION TO VALEO VBR
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