FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SIMMETRY SACROILIAC JOINT FUSION SYSTEM
K Number: K102907
·
Decision Dec 14, 2010
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
6
Review Days
74
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Basic Information
- Device Name
- SIMMETRY SACROILIAC JOINT FUSION SYSTEM
- K Number
- K102907
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Zyga Technology, Inc.
- Date Received
- October 1, 2010
- Decision Date
- December 14, 2010
- Product Code
- OUR
- 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 |
|---|---|---|---|
| OUR | Sacroiliac Joint Fixation | FDA class 2 | Orthopedic |
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Other Clearances by Zyga Technology, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K151818 | SImmetry Sacroiliac Joint Fusion System | Aug 5, 2015 | Substantially Equivalent |
| K141549 | SImmetry Sacroiliac Joint Fusion System | Jan 15, 2015 | Substantially Equivalent |
| K130092 | SIMMETRY SACROILIAC JOINT FUSION SYSTEM | Feb 27, 2013 | Substantially Equivalent |
| K111801 | SIMMETRY(TM) SACROILIAC JOINT FUSION SYSTEM | Jul 21, 2011 | Substantially Equivalent |
| K110512 | SIMMETRY SACROILIAC JOINT FUSION SYSTEM | Mar 23, 2011 | Substantially Equivalent |