JuggerStitch Meniscal Repair Device
FDA 510(k) K191459 · Biomet, Inc.
510(k) numberK191459
Submission
- Device name
- JuggerStitch Meniscal Repair Device
- Applicant
- Biomet, Inc.
Warsaw, IN, US - Received
- June 3, 2019
- Decision date
- September 13, 2019
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MBI – Fastener, Fixation, Nondegradable, Soft Tissue
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3040
- Specialty
- Orthopedic
- Implant
- Yes
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Questions and answers
When was JuggerStitch Meniscal Repair Device cleared by the FDA?
JuggerStitch Meniscal Repair Device (K191459) received a 510(k) decision of Substantially Equivalent on September 13, 2019, 102 days after the submission was received.
What is the product code of K191459?
The FDA product code is MBI – Fastener, Fixation, Nondegradable, Soft Tissue, a Class II (moderate risk) device regulated under 21 CFR 888.3040.