Mesh, Surgical, Deployer
FDA product code ORQ · 6 cleared devices
Class 2
General, Plastic Surgery
- Regulation
- 21 CFR 878.3300
- Review panel
- SU
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2010-06-17 – 2025-04-07
Intended to be used to facilitate the delivery of soft tissue prosthetics during the laparoscopic repair of soft tissue defects (e.G. Hernia repair).
ORQ
2025-04-07
ORQ
2013-04-05
ACCUMESH DEPLOYMENT SYSTEM
View details →
ORQ
2012-10-16
ACCUMESH DEPLOYMENT SYSTEM
View details →
ORQ
2012-05-02
ACCUMESH DEPLOYMENT SYSTEM
View details →
ORQ
2010-11-23
PATCHASSIST LARGE
View details →
ORQ
2010-06-17
PATCHASSIST
View details →No matching devices.
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