Arthrotek Meniscal Hybrid Device
FDA 510(k) K041988 · Biomet, Inc.
510(k) numberK041988
Submission
- Device name
- Arthrotek Meniscal Hybrid Device
- Applicant
- Biomet, Inc.
Warsaw, IN, US - Received
- July 23, 2004
- Decision date
- October 20, 2004
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JDR – Staple, Fixation, Bone
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3030
- Specialty
- Orthopedic
- Implant
- Yes
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Questions and answers
When was Arthrotek Meniscal Hybrid Device cleared by the FDA?
Arthrotek Meniscal Hybrid Device (K041988) received a 510(k) decision of Substantially Equivalent on October 20, 2004, 89 days after the submission was received.
What is the product code of K041988?
The FDA product code is JDR – Staple, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.