The following data is part of a premarket notification filed by Lima Intl. Corp. with the FDA for Muller Type Acetabular Cup.
Device ID | K900257 |
510k Number | K900257 |
Device Name: | MULLER TYPE ACETABULAR CUP |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
Applicant | LIMA INTL. CORP. 392 WAMPANOAG TRAIL E Providence, RI 02915 |
Contact | Pollonio-lister |
Correspondent | Pollonio-lister LIMA INTL. CORP. 392 WAMPANOAG TRAIL E Providence, RI 02915 |
Product Code | JDI |
CFR Regulation Number | 888.3350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-17 |
Decision Date | 1990-04-18 |