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

ORTHOVITA PEEK SPACER

K Number: K101171 · Decision Jan 25, 2011
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
23
Review Days
274

Basic Information

Device Name
ORTHOVITA PEEK SPACER
K Number
K101171
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthovita, Inc.
Date Received
April 26, 2010
Decision Date
January 25, 2011
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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