FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CRANK FRAME RETRACTOR
K Number: K882071
·
Decision Jun 10, 1988
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
42
Applicant Total
17
Review Days
24
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Basic Information
- Device Name
- CRANK FRAME RETRACTOR
- K Number
- K882071
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4800
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Karlin Technology, Inc.
- Date Received
- May 17, 1988
- Decision Date
- June 10, 1988
- Product Code
- GZT
- Advisory Committee
- Neurology
- 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 |
|---|---|---|---|
| GZT | Retractor, Self-Retaining, For Neurosurgery | FDA class 2 | Neurology |
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Other Clearances by Karlin Technology, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K903969 | SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RET | Sep 5, 1990 | Substantially Equivalent |
| K893201 | BONE PLATE | Apr 4, 1990 | Substantially Equivalent |
| K893203 | BONE SCREW | Apr 4, 1990 | Substantially Equivalent |
| K882525 | SPINAL MICROKNIFE | Sep 22, 1988 | Substantially Equivalent |
| K882519 | X-RAY MARKER | Aug 9, 1988 | Substantially Equivalent |
| K882520 | SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS | Jul 18, 1988 | Substantially Equivalent |
| K882073 | SPINAL NEEDLE | Jul 18, 1988 | Substantially Equivalent |
| K882524 | UNIVERSALLY ADJUSTABLE ARMBOARD | Jul 8, 1988 | Substantially Equivalent |
| K882069 | SPINAL DISTRACTORS, SPANNERS | Jun 17, 1988 | Substantially Equivalent |
| K882072 | ORTHOPAEDIC AND SPINAL RING CURRETTES | Jun 17, 1988 | Substantially Equivalent |