Nexmed Cancellous Bone Screws
FDA 510(k) K951656 · Nexmed, Inc.
510(k) numberK951656
Submission
- Device name
- Nexmed Cancellous Bone Screws
- Applicant
- Nexmed, Inc.
Palm Desert, CA, US - Received
- April 10, 1995
- Decision date
- July 18, 1995
- Decision
- Substantially Equivalent for Some Indications (SN)
- Type
- Traditional 510(k)
Device classification
- Product code
- HWC – Screw, Fixation, Bone
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3040
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code HWC
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261057 | ActivaScrew Cannulated COMHWC · Traditional | Bioretec, Ltd. | 09/04/2026SE |
| K260106 | OsteoCoil GT Active Compression SystemHWC · Traditional | Flower Orthopedics Corporation DBA Conventus… | 08/24/2026SE |
| K262344 | Large Compression ScrewsHWC · Special | TriMed, Inc. | 08/12/2026SE |
| K253858 | GFS - Sterile Screws and Top HatHWC · Special | T.A.G. Medical Products Corporation, Ltd. | 08/05/2026SE |
| K262075 | Lapidus Screw KitHWC · Special | Relja Innovations, LLC | 07/22/2026SE |
| K260809 | Arthrex Sterile VAL and VAL KreuLock Compression Screw SystemHWC · Traditional | Arthrex, Inc. | 06/25/2026SE |
| K253108 | VEOFIX Snap Off ScrewHWC · Traditional | Steps Ortho | 06/05/2026SE |
| K261154 | CoLink® & CoLag® Non-Sterile ScrewsHWC · Special | In2Bones USA, LLC | 05/30/2026SE |
| K261241 | TriMed Compression ScrewsHWC · Special | TriMed, Inc. | 05/14/2026SE |
| K254215 | Arthrex Beaming SystemHWC · Traditional | Arthrex, Inc. | 05/08/2026SE |
More from Arthrex, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K033580 | Nexflex Total Hip SystemLPH · Special | 08/05/2004SE |
| K991882 | Nexflex Total Knee SystemJWH · Traditional | 12/08/1999SE |
| K955171 | Nexlock Femoral StemJDG · Traditional | 02/09/1996SE |
| K955170 | Nexflex Femoral Stem, Standard DesignLPH · Traditional | 02/09/1996SE |
| K952629 | Nexflex Total Hip SystemJDI · Traditional | 09/08/1995SE |
Questions and answers
When was Nexmed Cancellous Bone Screws cleared by the FDA?
Nexmed Cancellous Bone Screws (K951656) received a 510(k) decision of Substantially Equivalent for Some Indications on July 18, 1995, 99 days after the submission was received.
What is the product code of K951656?
The FDA product code is HWC – Screw, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3040.