FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SECURE Screw
K Number: K191771
·
Decision Oct 16, 2019
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
6
Review Days
106
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Basic Information
- Device Name
- SECURE Screw
- K Number
- K191771
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- A.M. Surgical, Inc.
- Date Received
- July 2, 2019
- Decision Date
- October 16, 2019
- Product Code
- HWC
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | FDA class 2 | Orthopedic |
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Other Clearances by A.M. Surgical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K191345 | Pegasus System | Jul 17, 2019 | Substantially Equivalent |
| K180087 | A.M. Surgical Intramedullary Fixation Device | May 18, 2018 | Substantially Equivalent |
| K080133 | MOUNTABLE ENDOSCOPIC BLADE | Mar 13, 2008 | Substantially Equivalent |
| K042458 | A.M. SURGICAL CPF DISTAL RADIAL EXTERNAL CROSS PIN FIXATION SYSTEM | Oct 7, 2004 | Substantially Equivalent |
| K982142 | MOUNTABLE ENDOSCOPIC KNIFE | Dec 30, 1998 | Substantially Equivalent |