FDA 510(k) Applications Submitted by SIERRA M. MERTZ
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K202124 |
07/31/2020 |
Aesculap PAS-Port Proximal Anastomosis System |
Aesculap Inc. |
K192056 |
08/01/2019 |
JJ Series Container System |
Aesculap, Inc. |
K182414 |
09/04/2018 |
Aesculap« SterilContainer(TM) S2 System |
Aesculap, Inc. |
K222684 |
09/06/2022 |
XIA« 4.5 Spinal System, XIA« 4.5 Cortical Trajectory, XIA« 3 Spinal System, Serrato« Spinal System, XIA« Growth Rod Conversion Set, XIA« II Spinal System, XIA« Precision System, XIA« Anterior, Diapason« Spinal System, OpusÖ Spinal System, Radius« Spinal S |
Stryker Spine |
K193582 |
12/23/2019 |
SterilContainer S2 System |
Aesculap, Inc. |
K151772 |
06/30/2015 |
Actreen Mini Intermittent Urinary Catheters |
B. BRAUN MEDICAL INC. |
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