FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PATIENT CONTOURED MESH-PEEK (PCM-P)
K Number: K072707
·
Decision Dec 19, 2007
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
55
Applicant Total
58
Review Days
85
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Basic Information
- Device Name
- PATIENT CONTOURED MESH-PEEK (PCM-P)
- K Number
- K072707
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5330
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- KLS-Martin L.P.
- Date Received
- September 25, 2007
- Decision Date
- December 19, 2007
- Product Code
- GXN
- 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 |
|---|---|---|---|
| GXN | Plate, Cranioplasty, Preformed, Non-Alterable | FDA class 2 | Neurology |
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|---|---|---|---|
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