Atlas FDA

NEWDEAL COMPRESSION PLATES

FDA 510(k) clearance K093914 · decided 2011-04-14

Clearance details

K-number
K093914
Device name
NEWDEAL COMPRESSION PLATES
Applicant
Newdeal Sas
Decision
Substantially Equivalent
Date received
2009-12-22
Decision date
2011-04-14
Days to decision
478 days
Clearance type
Traditional
Product code
HRS
Device class
2
Regulation number
888.3030
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Planisboro, NJ, US
Third-party review
No
Expedited review
No

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Devices cleared under the same product code - the starting set for predicate research.

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SALGINA 2.5mm Distal Radius System (K261351)Bonebridge AG2026-06-26
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Recalls involving this device

RecordFirmDate
UNI-CP, Model Numbers: 330021S, 330023S, 330025S, 330030S, 330025S, 30030S, 330217S, 33022 recall (Z-2443-2018)NewDeal SA2018-07-16
ADVANSYS TTC, Model Numbers: 181011S, 181012S, 181013S, 181014S, 181001S, 181002S, 181003S recall (Z-2444-2018)NewDeal SA2018-07-16
ADVANSYS MLP/DLP, Model Numbers: 181051S, 181052S, 181041S, 181042S, 181031S, 181032S, 181 recall (Z-2445-2018)NewDeal SA2018-07-16
Large QWIX, Model Numbers: 111740S, 111745S, 111750S, 111755S, 111760S, 111765S, 111770S, recall (Z-2446-2018)NewDeal SA2018-07-16
TIBIAXYS, Model Numbers: 150010S, 150020S, 150030S, 150040S, 150120S, 150110S, 150130S, 15 recall (Z-2447-2018)NewDeal SA2018-07-16