FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

LIFE SPINE CEMENT RESTRICTOR

K Number: K060247 · Decision May 11, 2006
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
53
Applicant Total
36
Review Days
100

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Basic Information

Device Name
LIFE SPINE CEMENT RESTRICTOR
K Number
K060247
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Summary
Applicant
Life Spine
Date Received
January 31, 2006
Decision Date
May 11, 2006
Product Code
JDK
Advisory Committee
General, Plastic Surgery
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
JDK Prosthesis, Hip, Cement Restrictor

Similar 510(k) Clearances

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

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Other Clearances by Life Spine

K Number Device Name
K182470 Plateau Spacer System
K160169 The Life Spine Subtalar Implant System
K150368 Tarsa-Link Wedge Fixation System
K141905 PRO-LINK WEDGE SYSTEM
K133717 LONGBOW SPACER SYSTEM
K131077 LIFE SPINE PLATEAU SPACER SYSTEM
K123373 NAUTILUS SPINAL SYSTEM
K120998 SOLSTICE CROSS CONNECTOR
K111953 NAUTILUS SPINAL SYSTEM
K121116 PLATEAU SPACER SYSTEM
Search all 36 clearances from Life Spine →