FDA 510(k)
FDA class 2
Substantially Equivalent for Some Indications
🇺🇸 United States
KANEDA SR ANTERIOR SPINAL SYSTEM
K Number: K971248
·
Decision Jun 11, 1997
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
41
Review Days
69
Basic Information
- Device Name
- KANEDA SR ANTERIOR SPINAL SYSTEM
- K Number
- K971248
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3060
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent for Some Indications
- Applicant
- ACROMED CORP.
- Date Received
- April 3, 1997
- Decision Date
- June 11, 1997
- Product Code
- KWQ
- 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 |
|---|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | FDA class 2 | Orthopedic |
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Other Clearances by ACROMED CORP.
| K Number | Device Name | ||
|---|---|---|---|
| K980485 | ISOLA SPINAL SYSTEM | Oct 21, 1998 | Substantially Equivalent |
| K981714 | TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM | Jun 30, 1998 | Substantially Equivalent |
| K981113 | PEDIATRIC PRC | May 29, 1998 | Substantially Equivalent |
| K981274 | ACROMED TIMX PLATE BASED LOW BACK SYSTEM | Apr 29, 1998 | Substantially Equivalent |
| K980228 | UNIVERSITY PLATE ANTERIOR SYSTEM | Apr 14, 1998 | Substantially Equivalent for Some Indications |
| K974757 | KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS | Mar 5, 1998 | Substantially Equivalent for Some Indications |
| K972718 | M-2 ANTERIOR PLATE SYSTEM | Oct 1, 1997 | Substantially Equivalent for Some Indications |
| K970955 | ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM | Jun 11, 1997 | Substantially Equivalent for Some Indications |
| K970950 | EASY ROD | Jun 3, 1997 | Substantially Equivalent |
| K965102 | ACROMED PEDICLE SCREW | May 8, 1997 | Substantially Equivalent |