Atlas FDA

LAMINOPLASY PLATING SYSTEM

FDA 510(k) clearance K103284 · decided 2010-12-02

Clearance details

K-number
K103284
Device name
LAMINOPLASY PLATING SYSTEM
Applicant
Aesculap Implant Systems, Inc.
Decision
Substantially Equivalent
Date received
2010-11-05
Decision date
2010-12-02
Days to decision
27 days
Clearance type
Special
Product code
NQW
Device class
2
Regulation number
888.3050
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Center Valley, PA, US
Third-party review
No
Expedited review
No

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Life Spine Laminoplasty System (K181717)Life Spine, Inc.2018-10-12
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HAVEN™ Laminoplasty System, CANOPY® Laminoplasty Fixation System (K171413)Globus Medical, Inc.2017-07-14
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Recalls involving this device

No recalls on record reference this clearance.