FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HBS HEADLESS BONE SCREW
K Number: K020791
·
Decision Jun 6, 2002
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
5
Review Days
87
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Basic Information
- Device Name
- HBS HEADLESS BONE SCREW
- K Number
- K020791
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Millennium Medical Technologies, Inc.
- Date Received
- March 11, 2002
- Decision Date
- June 6, 2002
- 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 Millennium Medical Technologies, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K170449 | Autoclavable Suction Jar with Luer Lock extension - 250, 500, 1,000, 2,000 and 3,000 ml, Autoclavable Suction Jar without Luer Lock extension - 1,500 and 2,500 ml, Sterile 1,500 and 2,500 Lids with Conical patient connection 6-10 and overflow protection | Mar 31, 2017 | Substantially Equivalent |
| K081039 | LIPO CANNULA | Jul 10, 2008 | Substantially Equivalent |
| K031050 | PCW PERCUTANEOUS COMPRESSION WIRE | Jul 14, 2003 | Substantially Equivalent |
| K012294 | WRISTORE FIXATOR | Mar 4, 2002 | Substantially Equivalent |