The following data is part of a premarket notification filed by Covidien Llc with the FDA for Spacemaker Pro Access And Dissector System.
| Device ID | K151356 |
| 510k Number | K151356 |
| Device Name: | Spacemaker Pro Access And Dissector System |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | Covidien LLC 60 Middletown Avenue North Haven, CT 06473 |
| Contact | Rebecca Magnanimo |
| Correspondent | Rebecca Magnanimo Covidien LLC 60 Middletown Avenue North Haven, CT 06473 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-20 |
| Decision Date | 2015-06-18 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884521545332 | K151356 | 000 |
| 20884521545325 | K151356 | 000 |
| 20884521545318 | K151356 | 000 |
| 20884521545295 | K151356 | 000 |