The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Nexgen Prolong All-poly Patella.
| Device ID | K072281 |
| 510k Number | K072281 |
| Device Name: | NEXGEN PROLONG ALL-POLY PATELLA |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Contact | Brandon Hipsher |
| Correspondent | Brandon Hipsher ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-16 |
| Decision Date | 2007-09-06 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024215238 | K072281 | 000 |
| 00889024215221 | K072281 | 000 |
| 00889024215214 | K072281 | 000 |
| 00889024215207 | K072281 | 000 |
| 00889024215191 | K072281 | 000 |
| 00889024215184 | K072281 | 000 |