FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

TORQUE INSTRUMENT, MODEL 8500

K Number: K001476 · Decision Aug 4, 2000
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
31
Applicant Total
7
Review Days
85

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Basic Information

Device Name
TORQUE INSTRUMENT, MODEL 8500
K Number
K001476
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Spinalight, Inc.
Date Received
May 11, 2000
Decision Date
August 4, 2000
Product Code
LXM
Advisory Committee
Unknown
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LXM Manipulator, Plunger-Like Joint

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