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#
- 3015351976
- 2183449
- 9610905
- 1421101
- 1835998
- 3006460162
- 1221934
- 1834379
- 2080222
- 3012445569
- 3013497507
- 1836161
- 1030489
- 3004464325
- 3012725451
- 3007648354
- 8010303
- 3014257776
- 3043543260
- 8040179
- 1226544
- 3004571672
- 3005874553
- 3019455
- 3013846070
- 3011600579
- 2134947
- 3012234585
- 3015882686
- 2087382
- 3008711893
- 3003694247
- 3006001176
- 1056350
- 3016050940
- 1450781
- 9680718
- 3003477135
- 3009973505
- 8040278
- 1057425
- 3010009693
- 3010687973
- 3010303097
- 9617426
- 1935627
- 3005061536
- 3015542154
- 8010298
- 8010099
- 3006563559
- 3010386387
- 3016825318
- 9680825
- 3008285983
- 3012447612
- 3003120897
- 3009513193
- 1923569
- 3005440795
- 3031240334
- 8010379
- 3003393140
- 3007507973
- 1038671
- 3012130008
- 1020279
- 9615857
- 3004083789
- 3031481074
- 1828288
- 3003322138
- 1219655
- 3013784566
- 3009540749
- 3037407500
- 1822565
- 3012086398
- 3009888740
- 9613926
Source Documents#
510(k) summary PDF not indicated by FDA