ORTHOPAEDIC AND SPINAL RING CURRETTES
FDA 510(k) clearance K882072 · decided 1988-06-17
Clearance details
- K-number
- K882072
- Device name
- ORTHOPAEDIC AND SPINAL RING CURRETTES
- Applicant
- Karlin Technology, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-05-17
- Decision date
- 1988-06-17
- Days to decision
- 31 days
- Clearance type
- Traditional
- Product code
- JXH
- Device class
- 2
- Regulation number
- 882.5030
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Marina Del Rey, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| ANEUROPLASTIC, MODEL 43-1290 (K071776) | Codman & Shurtleff, Inc. | 2007-07-26 |
| ANEUROPLASTIC, ACRYLIC ANEURYOMORRHAPLY MATERIAL (K873688) | Dentsply Intl. | 1987-10-26 |
Recalls involving this device
No recalls on record reference this clearance.