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FDA 510(k) Applications Submitted by Paonan Biotech Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220261
01/31/2022
NEST-C Interbody System
Paonan Biotech Co., Ltd.
K180230
01/26/2018
NEST Interbody System
Paonan Biotech Co., Ltd.
K180226
01/26/2018
TREND II Spinal Fixation System- STEP Series
Paonan Biotech Co., Ltd.
K180228
01/26/2018
II-Type Intervertebral Spacer
Paonan Biotech Co., Ltd.
K182285
08/23/2018
PK High Tibial Osteotomy Correction System
Paonan Biotech Co., Ltd.
K161225
05/16/2016
Paonan Armstrong Posterior Spinal Fixation System
Paonan Biotech Co., Ltd.
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