FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN
K Number: K961522
·
Decision Sep 23, 1996
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
10
Review Days
154
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Basic Information
- Device Name
- KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN
- K Number
- K961522
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Synvasive Technology, Inc.
- Date Received
- April 22, 1996
- Decision Date
- September 23, 1996
- Product Code
- HTY
- 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 |
|---|---|---|---|
| HTY | Pin, Fixation, Smooth | FDA class 2 | Orthopedic |
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Other Clearances by Synvasive Technology, Inc.
| K Number | Device Name | ||
|---|---|---|---|
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| K070108 | ELIBRA DYNAMIC KNEE BALANCER | Apr 4, 2007 | Substantially Equivalent |
| K972508 | SURGICAL BURS AND SURGICAL DRILL BITS | Aug 26, 1997 | Substantially Equivalent |
| K950009 | POWERGRIP(TM) COMPRESSION FIXATION DEVICE | Aug 18, 1995 | Substantially Equivalent |
| K934336 | SPINALPLANE | Mar 10, 1995 | Substantially Equivalent for Some Indications |
| K933933 | CEBOPLANE | Apr 15, 1994 | Substantially Equivalent |
| K930573 | SYNVASIVE CERAMIC SUTTING BLOCK | Apr 7, 1994 | Substantially Equivalent |
| K932869 | ARTHROPLANE | Mar 25, 1994 | Substantially Equivalent |
| K931737 | HEDLEYL INTRAMEDULLARY PREPARATION BRUSH | Jan 7, 1994 | Substantially Equivalent |