Atlas FDA

TRIAL CABLE, 3009

FDA 510(k) clearance K070847 · decided 2007-04-11

Clearance details

K-number
K070847
Device name
TRIAL CABLE, 3009
Applicant
Advanced Neuromodulation Systems
Decision
Substantially Equivalent
Date received
2007-03-28
Decision date
2007-04-11
Days to decision
14 days
Clearance type
Special
Product code
GZB
Device class
2
Regulation number
882.5880
Medical specialty
Neurology
Advisory committee
Neurology
Location
Plano, TX, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.