510(k) K771744
- Device
- OSTEOTOMES FOR CUTTING BONH
- Applicant
- Depuy, Inc.
- 510(k) number
- K771744
- Product code
- HWM
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-09-28
- Date received
- 1977-09-15
- Regulation
- 878.4800
- Classification name
- Osteotome
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 4221 Richmond Rd., NW Walker MI US 49534 49534
FDA Registration Numbers#
- 9611616
- 3023657851
- 9611112
- 3008583793
- 3003322138
- 3005440795
- 9616671
- 3007507973
- 8010372
- 8010591
- 3011623994
- 3004215117
- 8043507
- 2249529
- 9615857
- 2431166
- 2087382
- 1526711
- 3015383864
- 2080222
- 1421879
- 1056350
- 3009703496
- 1834379
- 3016438694
- 8040278
- 3009051471
- 8010099
- 3010041511
- 1923569
- 3010687973
- 3003477135
- 1020279
- 3021723305
- 2183449
- 3015212339
- 3016825318
- 9681540
- 9611283
- 3009888740
- 1833053
- 3005751028
- 9613926
- 2134947
- 3006846753
- 3007597038
- 3010235355
- 3011015572
- 1226544
- 3002806535
- 3009959868
- 3013011598
- 9680718
- 3014257776
- 3002976036
- 3008850074
- 3009106092
- 1450781
- 3006142527
- 3010123256
- 1221934
- 1822565
- 3010699884
- 3009340886
- 3012507533
- 3015895045
- 3008749819
- 3014207283
- 8010523
- 1030489
- 8040179
- 3002862271
- 3002808270
- 3031481074
- 1032347
- 3001620590
- 3024988980
- 3012725451
- 3012267976
Source Documents#
510(k) summary PDF not indicated by FDA