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

LONGBOW SPACER SYSTEM

K Number: K133717 · Decision Sep 19, 2014
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
36
Review Days
288

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LONGBOW SPACER SYSTEM
K Number
K133717
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine
Date Received
December 5, 2013
Decision Date
September 19, 2014
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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

View all

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
K131077 LIFE SPINE PLATEAU SPACER SYSTEM
K123373 NAUTILUS SPINAL SYSTEM
K120998 SOLSTICE CROSS CONNECTOR
K111953 NAUTILUS SPINAL SYSTEM
K121116 PLATEAU SPACER SYSTEM
K113157 AILERON INTERSPINOUS FIXATION SYSTEM
Search all 36 clearances from Life Spine →