ISOROD PD-103 IMPLANT, MODEL ATI-PD-103— 510(k) K020683
Substantially EquivalentAti Medical, Inc.
FDA 510(k) clearance K020683 for ISOROD PD-103 IMPLANT, MODEL ATI-PD-103, Substantially Equivalent on 2002-12-17. Applicant: Ati Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Ati Medical, Inc.
- Product code
- Code KXK
- Device class
- Class 2
- Regulation
- 21 CFR 892.5730
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code KXK
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