Atlas FDA

LiquiBand Plus

FDA 510(k) clearance K183570 · decided 2020-03-09

Clearance details

K-number
K183570
Device name
LiquiBand Plus
Applicant
Advanced Medical Solutions Limited
Decision
Substantially Equivalent
Date received
2018-12-21
Decision date
2020-03-09
Days to decision
444 days
Clearance type
Traditional
Product code
MPN
Device class
2
Regulation number
878.4010
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Plymouth, GB
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
LIQUIFIX FIX8 Laparoscopic Hernia Mesh Fixation Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device (P220024/S004)Advanced Medical Solutions Limited2023-12-14
LIQUIFIX FIX8 Laparoscopic Hernia Mesh Fixation Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device (P220024/S001)Advanced Medical Solutions Limited2023-07-28
LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device (P220024)Advanced Medical Solutions Limited2023-06-02