Scaffold, Partial Medial Meniscal Defects Extending Into The Red/white Zone, Resorbable Bovine Collagen
General, Plastic Surgery · 21 CFR 878.3300
Intended for use in surgical procedures for the repair and reinforcement of soft tissue injuries of the medial meniscus. In repairing and reinforcing medial meniscal defects, the patient must have an intact meniscal rim and anterior and posterior horns for attachment of the mesh. In addition, the surgically prepared site must extend at least into the red/white zone of the meniscus to provide sufficient vascularization. The device reinforces soft tissue and provides a resorbable scaffold that is replaced by the patients own soft tissue. The device is not a prosthetic device and is not intended to replace normal body structure.
Recent MDR events
7 adverse event reports on file
- REJUVAKNEEJan 14, 2026InjuryCollagen Matrix, Inc.2249852-2026-00003
- XL CMI - MEDIALJul 1, 2019MalfunctionStryker Endoscopy-san Jose0002936485-2019-00267
- CMI - LATERALMay 8, 2019InjuryStryker Endoscopy-san Jose0002936485-2019-00195
- 9.0MM CMI - MEDIAL (INTERNATIONAL)Mar 21, 2018InjuryStryker Endoscopy-san Jose0002956141-2018-00001
- 9.0MM CMI - MEDIALDec 4, 2017InjuryStryker Endoscopy-san Jose0002956141-2017-00005
- MENAFLEX IMPLANT (MEDIAL)Jun 11, 2010InjuryRegen Biologics, Inc.2956141-2010-00002
- MENAFLEX IMPLANTJun 3, 2010InjuryRegen Biologics, Inc.2956141-2010-00001
Event type breakdown
Most-reported manufacturers
Recalls
1 recall events for this product code
Registered firms
7 firms currently registered for this product code