HWQ — Passer Class I
FDA Device Classification
Classification Details
- Product Code
- HWQ
- Device Class
- Class I
- Regulation Number
- 888.4540
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K970360 | mitek products | MITEK SUTURE RETROGRADER | March 10, 1997 |
| K923381 | acufex microsurgical | SOFT TISSUE EXPANDER | May 5, 1993 |
| K920621 | acufex microsurgical | ACUFEX PASSING PINS AND SURGICAL WIRE | May 5, 1993 |
| K885311 | instrument makar | MENISCUS MENDER II LOOP | February 9, 1989 |
| K843592 | visitec | VICO MICRO SURGICAL INSTRUMENTS | October 5, 1984 |
| K841623 | plastafil | SLOTTED SOFT-TISSUE INSTRUMENT | July 11, 1984 |
| K841622 | plastafil | SOFT-TISSUE INSTRUMENT | July 11, 1984 |
| K811679 | dow corning corp. healthcare industries materials | SILASTIC TENDON PASSER H.P. | July 10, 1981 |
| K791960 | 3m | ROTH-KENNEDY PASSER | October 4, 1979 |