FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PHALANGEAL FIXATION SYSTEM
K Number: K994232
·
Decision Mar 1, 2000
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
5
Review Days
76
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Basic Information
- Device Name
- PHALANGEAL FIXATION SYSTEM
- K Number
- K994232
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medcanica, Inc.
- Date Received
- December 16, 1999
- Decision Date
- March 1, 2000
- 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 Medcanica, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K011373 | INSTRUMENT DAMPING PORT | Oct 12, 2001 | Substantially Equivalent |
| K011349 | INTERCOSTAL LOCKABLE-DIRECTABLE PORT | Oct 5, 2001 | Substantially Equivalent |
| K991486 | ULTRA-CBX | Nov 5, 1999 | Substantially Equivalent |
| K991064 | METACARPAL FIXATION SYSTEM | Jun 23, 1999 | Substantially Equivalent |