FDA 510(k) Applications Submitted by PAUL AMUDALA

FDA 510(k) Number Submission Date Device Name Applicant
K210963 03/31/2021 ENNOVATE Spinal System Aesculap Implant Systems, LLC
K180914 04/09/2018 Aesculap Slim Clip Applier Aesculap, Inc.
K121403 05/10/2012 CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET TELEFLEX, INC.
K211572 05/21/2021 Aesculap Slim Clip Applier Aesculap, Inc
K141625 06/17/2014 POLYSYN SURGICAL SUTURE SURGICAL SPECIALTIES CORP.
K122027 07/11/2012 ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER ARROW INTERNATIONAL, INC.
K172235 07/25/2017 CoreHip« System Aesculap Implants Systems, LLC
K182032 07/30/2018 SterilContainer S System Aesculap, Inc.
K162134 08/01/2016 ENNOVATE Spinal System Aesculap Implant Systems, LLC
K122690 09/04/2012 ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE ARROW INTERNATIONAL, INC.
K162815 10/06/2016 SterilContainer S System AESCULAP, INC
K173271 10/12/2017 Aesculap Slim Clip Applier Forceps Aesculap, Inc.
K153396 11/24/2015 Aesculap OrthoPilot Next Generation AESCULAP IMPLANT SYSTEMS, LLC
K213871 12/13/2021 Ennovate Cervical Spinal and Occiput System Aesculap Implant Systems, LLC.
K103658 12/15/2010 FLEXTIP PLUS CLOSED TIP EPIDURAL CATHERTER TELEFLEX, INC.
K153700 12/23/2015 Aesculap(R) Implant Systems (AIS) S4 Navigation Instruments AESCULAP IMPLANT SYSTEMS, LLC


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