K242302
- 510(k) number
- K242302
- Device name
- RejuvaKnee Collagen Meniscus Implant
- Applicant
- Collagen Matrix, Inc. NJ · US
- Product code
- OLC — Scaffold, Partial Medial Meniscal Defects Extending
- Decision date
- 2024-10-02
- Date received
- 2024-08-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K242302.pdf
Official FDA record: K242302
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.