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

IDYS(TM) C

K Number: K130853 · Decision Nov 13, 2013
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
10
Review Days
230

Basic Information

Device Name
IDYS(TM) C
K Number
K130853
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clariance
Date Received
March 28, 2013
Decision Date
November 13, 2013
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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K240715 Idys® C ZP 3DTi
K220182 Aggeris™-C
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