The following data is part of a premarket notification filed by V. Mueller Neuro/spine with the FDA for Pacific Surgical Patties.
| Device ID | K993019 |
| 510k Number | K993019 |
| Device Name: | PACIFIC SURGICAL PATTIES |
| Classification | Neurosurgical Paddie |
| Applicant | V. MUELLER NEURO/SPINE 360 INDUSTRIAL RD., UNIT H San Carlos, CA 94070 |
| Contact | Terry Johnston |
| Correspondent | Terry Johnston V. MUELLER NEURO/SPINE 360 INDUSTRIAL RD., UNIT H San Carlos, CA 94070 |
| Product Code | HBA |
| CFR Regulation Number | 882.4700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-09-08 |
| Decision Date | 2000-03-30 |
| Summary: | summary |