510(k) K885305
- Device
- Acetabular Cup Pusher/impactor
- Applicant
- COBOT MEDICAL CORP.
- 510(k) number
- K885305
- Product code
- HXO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1989-02-08
- Date received
- 1988-12-27
- Regulation
- 888.4540
- Classification name
- Pusher, Socket
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- JACK QUINN
- Address
- P.O. Box 9216 Paramus NJ US 07653 07653
FDA Registration Numbers#
- 1219655
- 8030607
- 9612420
- 3010065126
- 3015487912
- 3005273623
- 1417592
- 3007539489
- 1649379
- 3013055499
- 3015516266
- 1219518
- 3000931034
- 1828464
- 9617297
- 3010536692
- 1818910
- 8043971
- 3000270450
- 3015399803
- 3017521423
- 3009554293
- 3005061536
- 3007410669
- 3026311512
- 3039169546
- 3038187464
- 3009973505
- 3006563559
- 2183449
- 3004371426
- 3014019090
- 3015383864
- 9611102
- 9616671
- 3010667733
- 3011513267
- 3016443334
- 9611827
- 3010303097
- 9613910
- 3015876273
- 3016438694
- 3015490794
- 9680059
- 3010071016
- 1822565
- 8010379
- 8040278
- 3010537287
- 3009106092
- 3006846753
- 3014207283
- 3009417901
- 3008812560
- 3004983210
- 1825034
- 1835572
- 1043534
- 3013846070
- 3014662844
- 1836161
- 1649390
- 2134947
- 9610612
- 3012130008
- 3005751028
- 3014938863
- 3004176895
- 3004049923
- 3010097171
- 3023852420
- 3007887127
- 1218882
Source Documents#
510(k) summary PDF not indicated by FDA