FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
METASURG SUBTALAR IMPLANT
K Number: K111265
·
Decision Aug 9, 2011
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
5
Review Days
97
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Basic Information
- Device Name
- METASURG SUBTALAR IMPLANT
- K Number
- K111265
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Metasurg
- Date Received
- May 4, 2011
- Decision Date
- August 9, 2011
- Product Code
- HWC
- 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 |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | FDA class 2 | Orthopedic |
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Other Clearances by Metasurg
| K Number | Device Name | ||
|---|---|---|---|
| K123926 | METASURG NITINOL STAPLE IMPLANT | May 3, 2013 | Substantially Equivalent |
| K111536 | METASURG DIGIFUSE IMPLANT | Jul 21, 2011 | Substantially Equivalent |
| K083469 | METASURG CANNULATED TIATANIUM HEMI IMPLANT, MODEL HM-1000 | Feb 13, 2009 | Substantially Equivalent |
| K070441 | METASURG SUBTALAR IMPLANT | May 8, 2007 | Substantially Equivalent |