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

ESPIN

K Number: K120553 · Decision Aug 9, 2012
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
8
Review Days
168

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Basic Information

Device Name
ESPIN
K Number
K120553
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nlt Spine, Ltd.
Date Received
February 23, 2012
Decision Date
August 9, 2012
Product Code
HRX
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
HRX Arthroscope

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Other Clearances by Nlt Spine, Ltd.

K Number Device Name
K153665 PROW FUSION-L
K153786 PROW FUSION-V
K151654 PROW FUSION
K133061 ESPIN SYSTEM
K130254 PROW FUSION
K130057 ESPIN
K112359 PROW FUSION