EXETER MESH
FDA 510(k) clearance K963940 · decided 1997-02-13
Clearance details
- K-number
- K963940
- Device name
- EXETER MESH
- Applicant
- Howmedica, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1996-10-01
- Decision date
- 1997-02-13
- Days to decision
- 135 days
- Clearance type
- Traditional
- Product code
- JDJ
- Device class
- 2
- Regulation number
- 878.3300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Rutherford, NJ, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Howmedica
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| LINK, ACETABULAR REVISION MESH CUP (K972760) | Link America, Inc. | 1997-10-22 |
| OSTEONICS RESTORATION ACETABULAR RING (K970957) | Osteonics Corp. | 1997-06-03 |
| REFLECTION ACETABULAR REINFORCEMENT RINGS (K962541) | Smith & Nephew Richards, Inc. | 1996-09-17 |
| PROTRUSION CAGES (K962007) | Depuy, Inc. | 1996-08-01 |
| OSTEONICS MICROSTRUCTURED ACETABULAR COMPONENTS (K925883) | Osteonics Corp. | 1993-06-15 |
| INTERMEDICS APR(TM) II FEMORAL COMPONENT (K890450) | Intermedics Orthopedics | 1989-08-09 |
Recalls involving this device
No recalls on record reference this clearance.