FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TRACTION ACCESSORIES
K Number: K823813
·
Decision Jan 14, 1983
Classifications
1
FEI Numbers
205
Registration Numbers
205
Same Product Code
37
Applicant Total
56
Review Days
28
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Basic Information
- Device Name
- TRACTION ACCESSORIES
- K Number
- K823813
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 888.5850
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Danek Medical, Inc.
- Date Received
- December 17, 1982
- Decision Date
- January 14, 1983
- Product Code
- HST
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HST | Apparatus, Traction, Non-Powered | FDA class 1 | Orthopedic |
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Other Clearances by Danek Medical, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K994122 | BONE GRAFT WASHER, MODEL 9090114 - 9090118 | Feb 18, 2000 | Substantially Equivalent |
| K993810 | CD HORIZON SPINAL SYSTEM | Feb 3, 2000 | Substantially Equivalent |
| K993855 | ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM | Dec 15, 1999 | Substantially Equivalent |
| K991528 | MODIFICATION TO TENOR SPINAL SYSTEM-ROD/BOLT CONNECTOR | May 28, 1999 | Substantially Equivalent |
| K990603 | MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM | Mar 10, 1999 | Substantially Equivalent |
| K982875 | MODIFICATION TO ZPLATE-ATL ANTERIOR FIXATION SYSTEM | Jan 19, 1999 | Substantially Equivalent |
| K984522 | MODIFICATION OF TSRH SPINAL SYSTEM | Jan 6, 1999 | Substantially Equivalent |
| K982154 | MODIFICATION OF TOWNLEY PEDICLE SCREW PLATING SYSTEM | Jul 13, 1998 | Substantially Equivalent |
| K970599 | TOWNLEY PEDICLE SCREW PLATING SYSTEM | Mar 20, 1998 | Substantially Equivalent |
| K943827 | SPINE FIXATION | Feb 14, 1996 | Substantially Equivalent for Some Indications |