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

ISOBAR SEMI-RIGID DUAL DAMPENER

K Number: K071261 · Decision Apr 17, 2008
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
21
Applicant Total
12
Review Days
349

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Basic Information

Device Name
ISOBAR SEMI-RIGID DUAL DAMPENER
K Number
K071261
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Scient'X
Date Received
May 4, 2007
Decision Date
April 17, 2008
Product Code
NQP
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
NQP Posterior Metal/Polymer Spinal System, Fusion

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