Mecron Cancellous Cannulated Bone Screws
FDA 510(k) K810205 · Serrano Intl.
510(k) numberK810205
Submission
- Device name
- Mecron Cancellous Cannulated Bone Screws
- Applicant
- Serrano Intl.
Mchenry, IL, US - Received
- January 26, 1981
- Decision date
- February 9, 1981
- Decision
- Substantially Equivalent (SESE)
- 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 |
|---|---|---|
| K851409 | Uniloc Total Hip Prosthesis · Traditional | 11/22/1985SE |
| K820899 | Mecron Voorhoeve Titanium Sheath · Traditional | 05/14/1982SE |
| K820619 | Mecron(R) Acetabular Nets TMFTM · Traditional | 05/14/1982SE |
| K820852 | Mecron Concavex Flexible IntramedullaryHSB · Traditional | 04/15/1982SE |
| K810497 | Bone Fixaction ScrewHWC · Traditional | 03/11/1981SE |
Questions and answers
When was Mecron Cancellous Cannulated Bone Screws cleared by the FDA?
Mecron Cancellous Cannulated Bone Screws (K810205) received a 510(k) decision of Substantially Equivalent on February 9, 1981, 14 days after the submission was received.
What is the product code of K810205?
The FDA product code is HWC – Screw, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3040.