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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